Johnson & Johnson Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Johnson & Johnson Medical, Inc. - FDA 510(k) Cleared Devices
53
Total
50
Cleared
0
Denied
Johnson & Johnson Medical, Inc. has 50 FDA 510(k) cleared medical devices. Based in Arlington, US.
Historical record: 50 cleared submissions from 1990 to 2000. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Johnson & Johnson Medical, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Johnson & Johnson Medical, Inc.
53 devices
Cleared
Jul 31, 2000
PROTECTIV SAFETY BLOOD COLLECTION NEEDLE
General Hospital
59d
Cleared
Mar 29, 1999
ADVANCED NIBP MODULE
Cardiovascular
243d
Cleared
Dec 16, 1998
NU-GEL * WOUND DRESSING
General & Plastic Surgery
83d
Cleared
Aug 20, 1998
FIBRCOL PLUS COLLAGEN WOUND DRESSING WITH ALGINATE
General & Plastic Surgery
27d
Cleared
May 18, 1998
CRITIKON SOFT BLOOD PRESSURE CUFF
Cardiovascular
201d
Cleared
Apr 28, 1998
I.V. CATHETER SYSTEM
General Hospital
78d
Cleared
Feb 17, 1998
OBSERVER * CENTRAL STATION
Cardiovascular
229d
Cleared
Dec 16, 1997
ULTRALON POWDER FREE LATEX SURGICAL GLOVE
General Hospital
78d
Cleared
Sep 19, 1997
DINAMAP MPS PORTABLE MONITOR
Cardiovascular
143d
Cleared
Aug 18, 1997
DINAMAP COMPACT MONITOR
Cardiovascular
213d
Cleared
Apr 16, 1997
HR POLYURETHANE PICC AND MIDLINE CATHETERS
General Hospital
154d
Cleared
Mar 21, 1997
DYNA-FLEX MULTI-LAYER COMPRESSION SYSTEM
General & Plastic Surgery
22d
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