FDA 510(k)

STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION

K-Number: K960003 · 1996-08-29

Decision Date1996-08-29

Product CodeHQC

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION is the device name listed in this FDA 510(k) record. The listed applicant is Storz Instrument Co.. It received FDA 510(k) clearance on 1996-08-29 under 510(k) number K960003. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION?

STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION is a medical device that received FDA 510(k) clearance on 1996-08-29. The listed applicant is Storz Instrument Co.. The 510(k) number is K960003.

When did STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION receive FDA 510(k) clearance?

STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION received FDA 510(k) clearance on 1996-08-29, under 510(k) number K960003.

Who is the listed applicant for STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION?

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

What is the FDA product code for STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION?

The FDA product code for STORZ D7116 MICROVIT VITRECTOMY CUTTER EXTENSION is HQC.

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Other records listing Storz Instrument Co. as applicant

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Related Devices (Code: HQC)

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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.