Procedure Products, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
FDA 510(k) Regulatory Record - Procedure Products, Inc. General Hospital ✕
8 devices
Cleared
Mar 27, 2017
Freedom Syringe
General Hospital
269d
Cleared
Apr 24, 1991
BAG SPIGOT
General Hospital
68d
Cleared
Dec 20, 1988
MODIFIED 10CC SYRINGE CONTROL RING SET
General Hospital
19d
Cleared
Feb 04, 1988
10CC SYRINGE CONTROL RING SET
General Hospital
78d
Cleared
Sep 05, 1984
DISPOSABLE STOPCOCKS
General Hospital
113d
Cleared
Apr 15, 1982
GLASS SYRINGES, DRUG, LUER LOCK
General Hospital
65d
Cleared
Oct 23, 1981
INJECTION CAP, LUER LOCK
General Hospital
35d
Cleared
May 21, 1981
MALE LUER LOCK PLUGS
General Hospital
45d