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FDA 510(k)

STORZ MICRO CUTTER 25 GAUGE PACK

K-Number: K913504 · 1992-02-21

ApplicantStorz
Decision Date1992-02-21
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STORZ MICRO CUTTER 25 GAUGE PACK is the device name listed in this FDA 510(k) record. The listed applicant is Storz. It received FDA 510(k) clearance on 1992-02-21 under 510(k) number K913504. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ MICRO CUTTER 25 GAUGE PACK?

STORZ MICRO CUTTER 25 GAUGE PACK is a medical device that received FDA 510(k) clearance on 1992-02-21. The listed applicant is Storz. The 510(k) number is K913504.

When did STORZ MICRO CUTTER 25 GAUGE PACK receive FDA 510(k) clearance?

STORZ MICRO CUTTER 25 GAUGE PACK received FDA 510(k) clearance on 1992-02-21, under 510(k) number K913504.

Who is the listed applicant for STORZ MICRO CUTTER 25 GAUGE PACK?

The FDA 510(k) record lists Storz as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for STORZ MICRO CUTTER 25 GAUGE PACK?

The FDA product code for STORZ MICRO CUTTER 25 GAUGE PACK is HQE.

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Other records listing Storz as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K960007STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATORK952151STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)K954340STORZ MICROFLOW PHACOEMULSIFICATION NEEDLEK930278STORZ COMPUSCAN ABK926512STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVE

Related Devices (Code: HQE)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K212763UniVit HE, UniVit UHSVisioncare Devices, LLCK170183Cetus system, Cetus probeA.R.C Laser GmbHK153168Bi-Blade Vitrectomy CutterMedical Instrument Development LaboratoriesK121675VERSAVITSynergetics, Inc.K120170PROCARE PLUS VITRECTOMY SYSTEMVisioncare Devices, Inc.K102222ULTIMATE VIT ENHAMCER (UVE)Medical Instrument Development Laboratories, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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