Shinemound Enterprise, Inc. - FDA 510(k) Cleared Devices
8
Total
8
Cleared
0
Denied
FDA 510(k) Regulatory Record - Shinemound Enterprise, Inc. General Hospital ✕
8 devices
Cleared
Sep 30, 2005
POWDERED LATEX PATIENT EXAMINATION GLOVES
General Hospital
77d
Cleared
Jan 28, 2000
SENSI-PRO, DISPOSABLE PRE-POWDERED SYNTHETIC VINYL PATIENT EXAMINATION GLOVES...
General Hospital
43d
Cleared
Jan 20, 2000
SENSI-PRO DISPOSABLE POWDER FREE SYNTHETIC VINYL PATIENT EXAMINATION GLOVES...
General Hospital
34d
Cleared
Oct 27, 1999
SENSI-PRO DISPOSABLE POWDERED VINYL SYNTHETIC EXAMINATION GLOVES WITH WHITE...
General Hospital
30d
Cleared
Oct 27, 1999
SENSI-PRO DISPOSABLE POWDER FREE VINYL SYNTHETIC EXAMINATION GLOVES WITH...
General Hospital
30d
Cleared
Dec 22, 1997
SYNTEX
General Hospital
255d
Cleared
Aug 15, 1997
LIGHTLY POWDERED VINYL SYNTHETIC EXAMINATION GLOVES
General Hospital
72d
Cleared
Mar 27, 1997
POLY-MED
General Hospital
36d