Walpak Co. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Walpak Co. - FDA 510(k) Cleared Devices
11
Total
10
Cleared
0
Denied
Walpak Co. has 10 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 10 cleared submissions from 1976 to 1981. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Walpak Co. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Walpak Co.
11 devices
Cleared
Jan 21, 1981
IRRIGATION SET W/BULB SYRINGE
General Hospital
35d
Cleared
Jan 21, 1981
IRRIGATION PISTON
General Hospital
35d
Cleared
Jan 15, 1981
IRRIGATION SET W/PISTON SYRINGE
General Hospital
29d
Cleared
Jan 15, 1981
SUTURE REMOVAL KIT
General & Plastic Surgery
29d
Cleared
Dec 17, 1980
LEMON GLYCERINE SWABS
General Hospital
Cleared
Sep 16, 1980
CATHETER INSERTION TRAY
Gastroenterology & Urology
18d
Cleared
Nov 16, 1979
CLOSED SYSTEM FOLEY CATHERIZATION PROCED
Gastroenterology & Urology
91d
Cleared
Feb 21, 1978
CATHETERIZATION PROCEDURE TRAY
Gastroenterology & Urology
28d
Cleared
Feb 21, 1978
CATHETERIZATION PROCED. TRAY, URETHRAL
Gastroenterology & Urology
28d
Cleared
Jun 15, 1977
SPONGES, LAPAROTOMY
General & Plastic Surgery
100d
Cleared
Nov 12, 1976
CATH CARE KIT
General Hospital
71d