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Stephens Instruments

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K022835STEPHENS DISPOSABLE FORCEPSNovember 1, 2002
K022836STEPHENS DISPOSABLE SPECULUMNovember 1, 2002
K022840STEPHENS DISPOSABLE SCISSORSNovember 1, 2002
K022842STEPHENS DISPOSABLE HOOKSNovember 1, 2002
K022843GAYHEART CORNEAL EXCISION DEVICENovember 1, 2002