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FDA 510(k)

FRAMES - VARIOUS BRAND NAMES

K-Number: K941767 · 1994-06-03

Decision Date1994-06-03
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FRAMES - VARIOUS BRAND NAMES is the device name listed in this FDA 510(k) record. The listed applicant is Lenscraft, Inc.. It received FDA 510(k) clearance on 1994-06-03 under 510(k) number K941767. 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 FRAMES - VARIOUS BRAND NAMES?

FRAMES - VARIOUS BRAND NAMES is a medical device that received FDA 510(k) clearance on 1994-06-03. The listed applicant is Lenscraft, Inc.. The 510(k) number is K941767.

When did FRAMES - VARIOUS BRAND NAMES receive FDA 510(k) clearance?

FRAMES - VARIOUS BRAND NAMES received FDA 510(k) clearance on 1994-06-03, under 510(k) number K941767.

Who is the listed applicant for FRAMES - VARIOUS BRAND NAMES?

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

What is the FDA product code for FRAMES - VARIOUS BRAND NAMES?

The FDA product code for FRAMES - VARIOUS BRAND NAMES is HQZ.

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.

Related Devices (Code: HQZ)

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.

Official Source

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