Snyder Laboratories, Inc. - FDA 510(k) Cleared Devices
16
Total
16
Cleared
0
Denied
Snyder Laboratories, Inc. has 16 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 16 cleared submissions from 1978 to 1984. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Snyder Laboratories, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Snyder Laboratories, Inc.
16 devices
Cleared
Nov 05, 1984
SNYDER HEMOVAC WOUND DRAINAGE DEVICES
General & Plastic Surgery
33d
Cleared
Aug 06, 1982
SNYDER DEBRIBEMENT SYSTEM LDP-1
General & Plastic Surgery
94d
Cleared
May 02, 1980
SNYDER HEMOVAC CHEST DRAINAGE SOLUTION
General Hospital
16d
Cleared
Apr 16, 1980
SNYDER HYSTERECTOMY Y TUBE KIT
General & Plastic Surgery
37d
Cleared
Apr 16, 1980
SNYDER HEMOVAC TM VENTED WOUND KIT
General & Plastic Surgery
33d
Cleared
Apr 16, 1980
SURGIVAC TM
General & Plastic Surgery
33d
Cleared
Apr 02, 1980
100 ML SNYDER HEMOVAC
General & Plastic Surgery
23d
Cleared
May 11, 1979
GREENLINE IRRIGATION TRAYS
General & Plastic Surgery
43d
Cleared
Apr 23, 1979
YANKAUER & POODLE SUCTION INSTRUMENTS
General Hospital
54d
Cleared
Apr 23, 1979
SUCTION CONNECTING TUBING
General Hospital
54d
Cleared
Apr 23, 1979
CATHETERS, GREENLINE SUCTION
Anesthesiology
25d
Cleared
Apr 10, 1979
URINARY DRAINAGE BAG
Gastroenterology & Urology
63d