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FDA 510(k)

OPHTHALMIC KNIFE

K-Number: K922378 · 1992-12-10

ApplicantMicroptics Development Laboratory
Decision Date1992-12-10
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPHTHALMIC KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Microptics Development Laboratory. It received FDA 510(k) clearance on 1992-12-10 under 510(k) number K922378. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPHTHALMIC KNIFE?

OPHTHALMIC KNIFE is a medical device that received FDA 510(k) clearance on 1992-12-10. The listed applicant is Microptics Development Laboratory. The 510(k) number is K922378.

When did OPHTHALMIC KNIFE receive FDA 510(k) clearance?

OPHTHALMIC KNIFE received FDA 510(k) clearance on 1992-12-10, under 510(k) number K922378.

Who is the listed applicant for OPHTHALMIC KNIFE?

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

What is the FDA product code for OPHTHALMIC KNIFE?

The FDA product code for OPHTHALMIC KNIFE is HNN.

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Related Devices (Code: HNN)

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.

K110166CLEARCUT S SAFETY KNIFEAlcon Research, Ltd.K882402RETRACTIVE INCISION MICROMETER (RIM) GUAGEOptical CenterK881669MVR/STILETTO BLADE 20GA. - P/N 1900Advanced Surgical Products, Inc.K874979PRISMA DISPOSABLE MVR/STILETTO BLADEAdvanced Surgical Products, Inc.K874057OPHTHALMIC TIP & BLADE SCALPELSMyocure, Inc.K874056OPHTHALMIC DISPOSABLE BLADESMyocure, 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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