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FDA 510(k)

SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS

K-Number: K870179 · 1987-04-22

ApplicantPolinelli
Decision Date1987-04-22
Product CodeHQZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS is the device name listed in this FDA 510(k) record. The listed applicant is Polinelli. It received FDA 510(k) clearance on 1987-04-22 under 510(k) number K870179. 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 SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS?

SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS is a medical device that received FDA 510(k) clearance on 1987-04-22. The listed applicant is Polinelli. The 510(k) number is K870179.

When did SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS receive FDA 510(k) clearance?

SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS received FDA 510(k) clearance on 1987-04-22, under 510(k) number K870179.

Who is the listed applicant for SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS?

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

What is the FDA product code for SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS?

The FDA product code for SPECTACLE FRAMES VARIOUS COLORS AND DESIGNS 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.

Other records listing Polinelli as applicant

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

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