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FDA 510(k)

RETRACTIVE INCISION MICROMETER (RIM) GUAGE

K-Number: K882402 · 1988-08-22

ApplicantOptical Center
Decision Date1988-08-22
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

RETRACTIVE INCISION MICROMETER (RIM) GUAGE is the device name listed in this FDA 510(k) record. The listed applicant is Optical Center. It received FDA 510(k) clearance on 1988-08-22 under 510(k) number K882402. 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 RETRACTIVE INCISION MICROMETER (RIM) GUAGE?

RETRACTIVE INCISION MICROMETER (RIM) GUAGE is a medical device that received FDA 510(k) clearance on 1988-08-22. The listed applicant is Optical Center. The 510(k) number is K882402.

When did RETRACTIVE INCISION MICROMETER (RIM) GUAGE receive FDA 510(k) clearance?

RETRACTIVE INCISION MICROMETER (RIM) GUAGE received FDA 510(k) clearance on 1988-08-22, under 510(k) number K882402.

Who is the listed applicant for RETRACTIVE INCISION MICROMETER (RIM) GUAGE?

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

What is the FDA product code for RETRACTIVE INCISION MICROMETER (RIM) GUAGE?

The FDA product code for RETRACTIVE INCISION MICROMETER (RIM) GUAGE 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.K922378OPHTHALMIC KNIFEMicroptics Development LaboratoryK881669MVR/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

View on FDA Database →

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

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