Johnson & Johnson Medical, Inc. - FDA 510(k) Cleared Devices
53
Total
50
Cleared
0
Denied
FDA 510(k) Regulatory Record - Johnson & Johnson Medical, Inc. General Hospital ✕
31 devices
Cleared
Jul 31, 2000
PROTECTIV SAFETY BLOOD COLLECTION NEEDLE
General Hospital
59d
Cleared
Apr 28, 1998
I.V. CATHETER SYSTEM
General Hospital
78d
Cleared
Dec 16, 1997
ULTRALON POWDER FREE LATEX SURGICAL GLOVE
General Hospital
78d
Cleared
Apr 16, 1997
HR POLYURETHANE PICC AND MIDLINE CATHETERS
General Hospital
154d
Cleared
Dec 23, 1996
PROTECTIV 2000 I.V. CATHETER SAFETY SYSTEM
General Hospital
196d
Cleared
Sep 20, 1996
MAXXUS POWDER FREE ORTHOPAEDIC LATEX SURGICAL GLOVES
General Hospital
50d
Cleared
Jul 03, 1996
MICRO-TOUCH POWDER FREE LATEX SURGICAL GLOVES
General Hospital
65d
Cleared
Oct 12, 1995
NEUTRALON BROWN LATEX SURGICAL GLOVES
General Hospital
69d
Cleared
Oct 05, 1995
MICRO-TOUCH* LATEX SURGICAL GLOVES
General Hospital
37d
Cleared
Sep 15, 1995
MAXXUS ORTHOPAEDIC SURGICAL GLOVES
General Hospital
42d
Cleared
Feb 13, 1995
MAXXUS LP ORTHOPAEDIC LATEX SURGICAL GLOVES
General Hospital
115d
Cleared
Feb 13, 1995
MICRO-TOUCH LP LATEX SURGICAL GLOVES
General Hospital
115d