The Urology Group

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K831703COVERUPSJanuary 3, 1984
K831489SURGICAL TUBE HOLDERDecember 12, 1983
K810739SUCTION WOUND DRAINAGE DEVICEJune 26, 1981
K810788SURGICAL TUBE HOLDERApril 17, 1981
K810787UROLOGIC TUBE HOLDERMarch 31, 1981
K801629COVER-ALL MALE INCONTINENCE DEVICEAugust 12, 1980