| FDA
Public Health Web Notification: Complications Related to the Use of Bone
Cement in Vertebroplasty and Kyphoplasty Procedures |
October
31, 2002 |
| PMA
Summary Information on Lea's Shield |
October
30, 2002 |
| Patient
Safety News Broadcast for October, 2002 |
October
29, 2002 |
| Summary
from the October 22, 2002 Circulatory System Devices Panel Meeting |
October
26, 2002 |
| MQSA
Facility Score Card |
October
25, 2002 |
| Premarket
Approval Applications Decisions Rendered for September 2002 |
October
25, 2002 |
| Summary
from the October 23, 2002 Circulatory System Devices Panel Meeting |
October
25, 2002 |
| International
Center Liaison Representative Roster - Revised |
October
24, 2002 |
| National
Center Liaison Representative Roster - Revised |
October
24, 2002 |
| Draft
Questions and Bibliography for the November 20-21 Orthopaedic and Rehabilitation
Devices Panel Meeting - Now Available |
October
22, 2002 |
| HHS
Welcomes Passage of Device User Fee Legislation - News Release |
October
21, 2002 |
| FDA/CDRH
Registered Foreign Establishments |
October
21, 2002 |
| Agenda,
Questions, Roster and Briefing Material for the October 22-23 Circulatory
System Devices Panel Meeting - Now Available |
October
21, 2002 |
| FDA
Public Health Web Notification: Cochlear Implant Recipients May Be At Greater
Risk for Meningitis - Updated |
October
17, 2002 |
| Survey
on the Reuse and Reprocessing of Single-Use Devices (SUDs) in U.S. Hospitals
- Executive Summary |
October
16, 2002 |
| Consumer
Information on: IMMULITE® Anti-HBc and IMMULITE® 2000 Anti-HBc |
October
11, 2002 |
| Consumer
Information on : Neuroform(tm) Microdelivery Stent System |
October
11, 2002 |
| Announcement
of Upcoming Meeting of the Orthopaedic and Rehabilitation Devices Panel
- November 20 - 21, 2002 |
October
10, 2002 |
| Consumer
Information on: IMMULITE® HBsAg and IMMULITE® 2000 HBsAg and Confirmatory
Kit |
October
10, 2002 |
| Consumer
Information on: IMMULITE® Anti-HBc IgM and IMMULITE® 2000 Anti-HBc
IgM |
October
10, 2002 |
| The Radiological
Devices Panel meeting originally scheduled for October 16th, 2002, is being
rescheduled, by mutual agreement between FDA and the sponsor, for administrative
and logistical reasons. A new panel meeting date will be posted as soon
as possible. |
October
9, 2002 |
| Consumer
Information on : IMMULITE Anti-HBs and IMMULITE 2000 Anti-HBs |
October
9, 2002 |
| Patient
Informed Decision Labeling for Saline-Filled Breast Implants - Inamed Aesthetics-
Updated |
October
8, 2002 |
User
Facility Reporting Bulletin - Fall issue.
This issue contains an important article on monitoring temporary pacemaker
connections. Also featured are articles on selecting a third-party reprocessor
for single-use devices and hazards in patient-controlled analgesia, an FDA
public health notification about human tissue processed by Cryolife, Inc.,
and an announcement of the latest program topics for the September 2002
FDA Patient Safety News broadcast.
|
October
7, 2002 |
| Patient
Informed Decision Labeling for Saline-Filled Breast Implants - Mentor Corporation
- Updated |
October
7, 2002 |
| 510(k)
Decisions Rendered for September 2002 |
October
7, 2002 |
| Blue
Book Memo - Intercenter Consultative/Collaborative Review Process (G02-1) |
October
4, 2002 |
| FDA
Public Health Web Notification: Cochlear Implant Recipients may be at Greater
Risk for Meningitis - Updated |
October
4, 2002 |
| FDA
Public Health Web Notification: Cochlear Implant Recipients may be at Greater
Risk for Meningitis - Updated |
October
3, 2002 |
| Minutes
for the National Mammography Quality Assurance Advisory Committee -- August
26, 2002 |
October
1, 2002 |
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