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FDA 510(k)

GLASS FRAMES & COMPONENT PARTS

K-Number: K831388 · 1983-06-02

ApplicantAnamar
Decision Date1983-06-02
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

GLASS FRAMES & COMPONENT PARTS is the device name listed in this FDA 510(k) record. The listed applicant is Anamar. It received FDA 510(k) clearance on 1983-06-02 under 510(k) number K831388. 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 GLASS FRAMES & COMPONENT PARTS?

GLASS FRAMES & COMPONENT PARTS is a medical device that received FDA 510(k) clearance on 1983-06-02. The listed applicant is Anamar. The 510(k) number is K831388.

When did GLASS FRAMES & COMPONENT PARTS receive FDA 510(k) clearance?

GLASS FRAMES & COMPONENT PARTS received FDA 510(k) clearance on 1983-06-02, under 510(k) number K831388.

Who is the listed applicant for GLASS FRAMES & COMPONENT PARTS?

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

What is the FDA product code for GLASS FRAMES & COMPONENT PARTS?

The FDA product code for GLASS FRAMES & COMPONENT PARTS 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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