Storz

FDA Regulatory Profile

Summary

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

Recent 510(k) Clearances

K-NumberDeviceDate
K960007STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATORMarch 26, 1996
K952151STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)March 4, 1996
K954340STORZ MICROFLOW PHACOEMULSIFICATION NEEDLEDecember 14, 1995
K930278STORZ COMPUSCAN ABFebruary 9, 1994
K926512STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVESeptember 9, 1993
K913504STORZ MICRO CUTTER 25 GAUGE PACKFebruary 21, 1992