Johnson & Johnson Medical, Inc. - FDA 510(k) Cleared Devices
53
Total
50
Cleared
0
Denied
FDA 510(k) Regulatory Record - Johnson & Johnson Medical, Inc. Cardiovascular ✕
7 devices
Cleared
Mar 29, 1999
ADVANCED NIBP MODULE
Cardiovascular
243d
Cleared
May 18, 1998
CRITIKON SOFT BLOOD PRESSURE CUFF
Cardiovascular
201d
Cleared
Feb 17, 1998
OBSERVER * CENTRAL STATION
Cardiovascular
229d
Cleared
Sep 19, 1997
DINAMAP MPS PORTABLE MONITOR
Cardiovascular
143d
Cleared
Aug 18, 1997
DINAMAP COMPACT MONITOR
Cardiovascular
213d
Cleared
Jan 07, 1997
CCENTERMARK CATHETER INTRODUCER SHEALTH WITH PROTECTIV 2000 NEEDLE SAFETY SYSTEM
Cardiovascular
160d
Cleared
Aug 15, 1996
DINAMAP SELECT MULTI-PARAMETER SYSTEM
Cardiovascular
281d