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Bryan Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K002063BIOTRACE, MODEL 1730August 10, 2000
K913242MICROPROCESSED CONTROLLED LAPAROFLATORSeptember 25, 1992
K894380DUMON TRACHEOBRONCHIAL STENTOctober 24, 1989
K881249BAGGISH, HYSTEROSCOPEJuly 28, 1988
K854414DUMON/HARRELLMarch 12, 1986