Johnson & Johnson Medical, Div. of Ethicon, Inc. is one of 13140 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Johnson & Johnson Medical, Div. of Ethicon, Inc. - FDA 510(k) Cleared...
Recent clearances: MODIFICATION OF JELCO*,JELCO*-W AND JELCO* PLUS I.V. CATHETERS, CATHLON* I.V. CATHETERS, OPTIVA* I.V. CATHETERS, PROTECT, BARRIER SURGICAL GOWNS, NEUTRALON PF POWDER FREE BROWN LATEX SURGICAL GLOVES
5
Total
5
Cleared
0
Denied
Johnson & Johnson Medical, Div. of Ethicon, Inc. has 5 FDA 510(k) cleared medical devices. Based in Arlington, US.
Historical record: 5 cleared submissions from 1998 to 1999. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Johnson & Johnson Medical, Div. of Ethicon, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Johnson & Johnson Medical, Div. of Ethicon, Inc.
5 devices
Cleared
Aug 20, 1999
MODIFICATION OF JELCO*,JELCO*-W AND JELCO* PLUS I.V. CATHETERS, CATHLON* I.V....
General Hospital
207d
Cleared
Apr 13, 1999
BARRIER SURGICAL GOWNS
General Hospital
63d
Cleared
Nov 30, 1998
NEUTRALON PF POWDER FREE BROWN LATEX SURGICAL GLOVES
General Hospital
76d
Cleared
Nov 25, 1998
TIELLE PLUS HYDROPOLYMER ADHESIVE DRESSING
General & Plastic Surgery
71d
Cleared
Nov 03, 1998
MODIFICATION TO TIELLE HYDROPOLMER DRESSING
General & Plastic Surgery
39d