Molnlycke Health Care, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Molnlycke Health Care, Inc. - FDA 510(k) Cleared Devices
10
Total
9
Cleared
0
Denied
Molnlycke Health Care, Inc. has 9 FDA 510(k) cleared medical devices. Based in Eddystone, US.
Historical record: 9 cleared submissions from 1998 to 2006. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Molnlycke Health Care, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Molnlycke Health Care, Inc.
10 devices
Cleared
Oct 05, 2006
POWDER FREE STERILE NITRILE EXAMINATION GLOVES, BLUE
General Hospital
71d
Cleared
Jul 14, 2005
BARRIER SURGICAL DRAPES
General Hospital
24d
Cleared
Jul 11, 2000
KLINIDRAPE REINFORCED SURGICAL GOWNS
General Hospital
112d
Cleared
Jul 05, 2000
KLINIDRAPE SURGICAL GOWNS, NON-REINFORCED, BASIC PROTECTIONS AND STANDARD...
General Hospital
106d
Cleared
Jun 23, 2000
KLINIDRAPE SURGICAL DRAPES
General Hospital
94d
Cleared
Mar 03, 1999
MEPITEL NON ADHERENT SILICONE DRESSING
General & Plastic Surgery
86d
Cleared
Mar 01, 1999
HYPERGEL 20% HYPERTONIC SALINE GEL
General & Plastic Surgery
84d
Cleared
Feb 22, 1999
NORMLGEL 0.9% ISOTONIC SALINE GEL
General & Plastic Surgery
77d
Cleared
Nov 10, 1998
ALLDRESS, ABSORBENT FILM DRESSING
General & Plastic Surgery
28d
Cleared
Oct 28, 1998
MEPILEX
General & Plastic Surgery
47d