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FDA 510(k)

CALIFORNIA CONVERTIBLES (SUNGLASSES)

K-Number: K880709 · 1988-04-01

Decision Date1988-04-01
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CALIFORNIA CONVERTIBLES (SUNGLASSES) is the device name listed in this FDA 510(k) record. The listed applicant is Jmj World Trade Corp.. It received FDA 510(k) clearance on 1988-04-01 under 510(k) number K880709. 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 CALIFORNIA CONVERTIBLES (SUNGLASSES)?

CALIFORNIA CONVERTIBLES (SUNGLASSES) is a medical device that received FDA 510(k) clearance on 1988-04-01. The listed applicant is Jmj World Trade Corp.. The 510(k) number is K880709.

When did CALIFORNIA CONVERTIBLES (SUNGLASSES) receive FDA 510(k) clearance?

CALIFORNIA CONVERTIBLES (SUNGLASSES) received FDA 510(k) clearance on 1988-04-01, under 510(k) number K880709.

Who is the listed applicant for CALIFORNIA CONVERTIBLES (SUNGLASSES)?

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

What is the FDA product code for CALIFORNIA CONVERTIBLES (SUNGLASSES)?

The FDA product code for CALIFORNIA CONVERTIBLES (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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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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