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Thomas J. Fogarty, M.D.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K902453OSCILLOMETRIC PULSE DETECTION DEVICEAugust 23, 1990
K884154TRANSLUMINAL ENDARTERECTOMY DEVICEDecember 27, 1988
K831809FOGARTY OCCLUDER PADAugust 27, 1984
K841310GASTROINTESTINAL DILATORJuly 31, 1984
K834451COAXIAL BALLOON GASTROESOPHAGEAL DILAFebruary 4, 1984
K831384COAXIAL BALLOON URETHRAL DILATORJuly 26, 1983