Frantz Medical Development, Ltd. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Frantz Medical Development, Ltd. - FDA 510(k) Cleared Devices
5
Total
4
Cleared
0
Denied
Frantz Medical Development, Ltd. has 4 FDA 510(k) cleared medical devices. Based in New York, US.
Historical record: 4 cleared submissions from 1987 to 1998. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Frantz Medical Development, Ltd. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Frantz Medical Development, Ltd.
5 devices
Cleared
Aug 13, 1998
CLEARSTAR ENTERAL NUTRITION PUMP
General Hospital
106d
Cleared
Mar 19, 1991
ENDOSCOPIC ACCESSORY TO THE LIGHT SOURCE
Gastroenterology & Urology
116d
Cleared
Nov 05, 1987
FLEXIFLO COMPANION ENTERAL NUTRITION PUMP
General Hospital
87d
Cleared
Aug 10, 1987
BIOPSY FORCEPS
Gastroenterology & Urology
101d
Cleared
Feb 06, 1987
FRANTZ MEDICAL ELECTRODE
Cardiovascular
150d