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FDA 510(k)

REWINNER ENT CO. LTD. NON-PRESCRIPTION SUNGLASSES

K-Number: K940830 · 1994-04-11

Decision Date1994-04-11
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

REWINNER ENT CO. LTD. NON-PRESCRIPTION SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Rainbow Merchandise, Inc.. It received FDA 510(k) clearance on 1994-04-11 under 510(k) number K940830. 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 REWINNER ENT CO. LTD. NON-PRESCRIPTION SUNGLASSES?

REWINNER ENT CO. LTD. NON-PRESCRIPTION SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-04-11. The listed applicant is Rainbow Merchandise, Inc.. The 510(k) number is K940830.

When did REWINNER ENT CO. LTD. NON-PRESCRIPTION SUNGLASSES receive FDA 510(k) clearance?

REWINNER ENT CO. LTD. NON-PRESCRIPTION SUNGLASSES received FDA 510(k) clearance on 1994-04-11, under 510(k) number K940830.

Who is the listed applicant for REWINNER ENT CO. LTD. NON-PRESCRIPTION SUNGLASSES?

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

What is the FDA product code for REWINNER ENT CO. LTD. NON-PRESCRIPTION SUNGLASSES?

The FDA product code for REWINNER ENT CO. LTD. 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.

Other records listing Rainbow Merchandise, Inc. 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: 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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