ClearanceBrief
Company ยท US

Storz

FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 1996. Name variants (Inc, Corp, punctuation) are merged.

6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
HQCUnit, Phacofragmentation2
HQEInstrument, Vitreous Aspiration And Cutting, Ac-Powered1
HQRApparatus, Cautery, Radiofrequency, Ac-Powered1
IYOSystem, Imaging, Pulsed Echo, Ultrasonic1
MPAEndoilluminator1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 26, 1996K960007STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR
Storz
MPA
Mar 4, 1996K952151STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)
Storz
HQR
Dec 14, 1995K954340STORZ MICROFLOW PHACOEMULSIFICATION NEEDLE
Storz
HQC
Feb 9, 1994K930278STORZ COMPUSCAN AB
Storz
IYO
Sep 9, 1993K926512STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE
Storz
HQC
Feb 21, 1992K913504STORZ MICRO CUTTER 25 GAUGE PACK
Storz
HQE

Latest recalls

DateFirm and productCodeLinked 510(k)
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