Diamed Division Ill. Tool Works, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Diamed Division Ill. Tool Works, Inc. - FDA 510(k) Cleared Devices
7
Total
7
Cleared
0
Denied
Diamed Division Ill. Tool Works, Inc. has 7 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 7 cleared submissions from 1978 to 1986. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Diamed Division Ill. Tool Works, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Diamed Division Ill. Tool Works, Inc.
7 devices
Cleared
Apr 22, 1986
DIAMED MODELS 600, 900, 960, 964
Radiology
133d
Cleared
Dec 28, 1982
FEMALE EXTERNAL URINARY APPLIANCE
Gastroenterology & Urology
41d
Cleared
Oct 13, 1981
TOUCHLESS HOME-CATH
Gastroenterology & Urology
61d
Cleared
Nov 12, 1980
URINARY DRAINAGE UNT
Gastroenterology & Urology
15d
Cleared
Nov 12, 1980
TOUCHLESS CLEAN-CATH
Gastroenterology & Urology
15d
Cleared
Jun 01, 1979
TOUCHLESS TM FOLEY CATHETER KIT
Gastroenterology & Urology
49d
Cleared
Aug 31, 1978
STERILE URETHRAL CATHETER KIT
Gastroenterology & Urology
674d