Smith & Nephew Perry is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Smith & Nephew Perry - FDA 510(k) Cleared Devices
10
Total
10
Cleared
0
Denied
Smith & Nephew Perry has 10 FDA 510(k) cleared general hospital devices. Based in Massillon, US.
Historical record: 10 cleared submissions from 1991 to 1993.
Browse the complete list of FDA 510(k) cleared general hospital devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Smith & Nephew Perry
10 devices
Cleared
Dec 22, 1993
ENCORE POWDER-FREE SURGICAL GLOVES ORTHOPAEDIA
General Hospital
203d
Cleared
Dec 22, 1993
ENCORE POWDER-FREE SURGICAL GLOVES MICROPTIC
General Hospital
203d
Cleared
Nov 18, 1993
PERRY ENHANCED PROTECTION LATEX SURGICAL GLOVE
General Hospital
244d
Cleared
Feb 10, 1993
PERRY POWDER-FREE GLOVES, STYLE 45G
General Hospital
189d
Cleared
Sep 22, 1992
STERILE LATEX EXAMINATION GLOVES
General Hospital
125d
Cleared
Apr 22, 1992
PERRY(R) NATURAL POWDER-FREE GLOVES, STYLE 45
General Hospital
201d
Cleared
Jan 31, 1992
PERRY(R) CUT-RESISTANT GLOVES
General Hospital
88d
Cleared
Oct 02, 1991
PERRY(R) DERMAGUARD(R) PLUS GLOVES
General Hospital
64d
Cleared
May 09, 1991
PERRY(R) ENCORE CHEMOTHERAPY GLOVE
General Hospital
28d
Cleared
Jan 11, 1991
PERRY XTENDA CUFF SURGICAL GLOVES
General Hospital
31d