Thomas J. Fogarty, M.D. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Thomas J. Fogarty, M.D. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Thomas J. Fogarty, M.D. has 6 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 6 cleared submissions from 1983 to 1990. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Thomas J. Fogarty, M.D. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Thomas J. Fogarty, M.D.
6 devices
Cleared
Aug 23, 1990
OSCILLOMETRIC PULSE DETECTION DEVICE
Cardiovascular
83d
Cleared
Dec 27, 1988
TRANSLUMINAL ENDARTERECTOMY DEVICE
Gastroenterology & Urology
85d
Cleared
Aug 27, 1984
FOGARTY OCCLUDER PAD
Cardiovascular
448d
Cleared
Jul 31, 1984
GASTROINTESTINAL DILATOR
Gastroenterology & Urology
123d
Cleared
Feb 04, 1984
COAXIAL BALLOON GASTROESOPHAGEAL DILA
Gastroenterology & Urology
47d
Cleared
Jul 26, 1983
COAXIAL BALLOON URETHRAL DILATOR
Gastroenterology & Urology
89d