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FDA 510(k)

FRAMES, SPECTACLES

K-Number: K932772 · 1993-09-20

ApplicantOptical Designs and Sourcing, Inc.
Decision Date1993-09-20
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FRAMES, SPECTACLES is the device name listed in this FDA 510(k) record. The listed applicant is Optical Designs and Sourcing, Inc.. It received FDA 510(k) clearance on 1993-09-20 under 510(k) number K932772. 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, SPECTACLES?

FRAMES, SPECTACLES is a medical device that received FDA 510(k) clearance on 1993-09-20. The listed applicant is Optical Designs and Sourcing, Inc.. The 510(k) number is K932772.

When did FRAMES, SPECTACLES receive FDA 510(k) clearance?

FRAMES, SPECTACLES received FDA 510(k) clearance on 1993-09-20, under 510(k) number K932772.

Who is the listed applicant for FRAMES, SPECTACLES?

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

What is the FDA product code for FRAMES, SPECTACLES?

The FDA product code for FRAMES, SPECTACLES is HQZ.

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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.

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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.

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