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FDA 510(k)

STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR

K-Number: K960007 · 1996-03-26

ApplicantStorz
Decision Date1996-03-26
Product CodeMPA
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR is the device name listed in this FDA 510(k) record. The listed applicant is Storz. It received FDA 510(k) clearance on 1996-03-26 under 510(k) number K960007. The device is classified under product code MPA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR?

STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR is a medical device that received FDA 510(k) clearance on 1996-03-26. The listed applicant is Storz. The 510(k) number is K960007.

When did STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR receive FDA 510(k) clearance?

STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR received FDA 510(k) clearance on 1996-03-26, under 510(k) number K960007.

Who is the listed applicant for STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR?

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 MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR?

The FDA product code for STORZ MVS 1011A DISPOSABLE FIBEROPTIC ENDOILLUMINATOR is MPA.

Related Clinical Trials

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.

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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.

K952151STORZ OPHTHALMIC BIPOLAR CAUTERY INSTRUMENTS (D8200, D8201, D8203) AND BIPOLAR CORDS (D8202, D8204)K954340STORZ MICROFLOW PHACOEMULSIFICATION NEEDLEK930278STORZ COMPUSCAN ABK926512STORZ MODIFIED PHACO NEEDLE WITH INSULATION SLEEVEK913504STORZ MICRO CUTTER 25 GAUGE PACK

Related Devices (Code: MPA)

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.

K253468Nova Eye iTrack™ 250A Canaloplasty Microcatheter (iTrack™ 250A)Nova Eye, Inc.K242184Alcon 27GA Chandelier (8065000252); Alcon 27+ DS Wide Angle Endoilluminator (8065000253); Alcon 27+ DS Endoilluminator (8065000256);Alcon Laboratories, Inc.K233653Midfield Light Pipe, 23ga (3269.M06-00); Midfield Light Pipe, 25ga (3269.M05-00); Midfield Light Pipe, 27ga (3269.M04-00)Peregrine Surgical, LLCK221872ITrack Advance Canaloplasty Microcatheter with Advanced Delivery SystemNova Eye Inc. (Business Name Nova Eye Medical)K202670Nam illumination probe with chopperOculight , Ltd.K080067ISCIENCE INTERVENTIONAL OPHTHALMIC MICROCATHETERIscience Interventional

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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