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Hirata Sangyo Co. USA, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
8
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K864106SR-MODEL 230 (MODIFICATION)November 19, 1986
K842289SR- MODEL 230July 25, 1984
K833541SURGICAL INSTRUMENTNovember 28, 1983
K833542SURGICAL INSTRUMENTNovember 28, 1983
K832686MULTIPLE MANUAL SURGICAL INSTRUMENTSOctober 14, 1983
K831583GP-303July 19, 1983
K821989NON-STETHO 7, UM-15TPOctober 18, 1982
K822571SYRINGE PUMPOctober 8, 1982