FDA 510(k)

MEMLITE (PLASTIC EYEGLASS FRAMES)

K-Number: K770221 · 1977-02-17

Decision Date1977-02-17

Product CodeHQZ

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

MEMLITE (PLASTIC EYEGLASS FRAMES) is the device name listed in this FDA 510(k) record. The listed applicant is American Optical Corp.. It received FDA 510(k) clearance on 1977-02-17 under 510(k) number K770221. The device is classified under product code HQZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEMLITE (PLASTIC EYEGLASS FRAMES)?

MEMLITE (PLASTIC EYEGLASS FRAMES) is a medical device that received FDA 510(k) clearance on 1977-02-17. The listed applicant is American Optical Corp.. The 510(k) number is K770221.

When did MEMLITE (PLASTIC EYEGLASS FRAMES) receive FDA 510(k) clearance?

MEMLITE (PLASTIC EYEGLASS FRAMES) received FDA 510(k) clearance on 1977-02-17, under 510(k) number K770221.

Who is the listed applicant for MEMLITE (PLASTIC EYEGLASS FRAMES)?

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

What is the FDA product code for MEMLITE (PLASTIC EYEGLASS FRAMES)?

The FDA product code for MEMLITE (PLASTIC EYEGLASS FRAMES) is HQZ.

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Other records listing American Optical Corp. as applicant

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Related Devices (Code: HQZ)

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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.