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FDA 510(k)

FOSTER GRANT NON PRESCRIPTION SUNGLASSES

K-Number: K953092 · 1995-07-19

Decision Date1995-07-19
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FOSTER GRANT NON PRESCRIPTION SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Foster Grant Group. It received FDA 510(k) clearance on 1995-07-19 under 510(k) number K953092. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FOSTER GRANT NON PRESCRIPTION SUNGLASSES?

FOSTER GRANT NON PRESCRIPTION SUNGLASSES is a medical device that received FDA 510(k) clearance on 1995-07-19. The listed applicant is Foster Grant Group. The 510(k) number is K953092.

When did FOSTER GRANT NON PRESCRIPTION SUNGLASSES receive FDA 510(k) clearance?

FOSTER GRANT NON PRESCRIPTION SUNGLASSES received FDA 510(k) clearance on 1995-07-19, under 510(k) number K953092.

Who is the listed applicant for FOSTER GRANT NON PRESCRIPTION SUNGLASSES?

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

What is the FDA product code for FOSTER GRANT NON PRESCRIPTION SUNGLASSES?

The FDA product code for FOSTER GRANT NON PRESCRIPTION SUNGLASSES is HQY.

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: HQY)

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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