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FDA 510(k)

STYLE I WRAPPER SUNGLASSES

K-Number: K943405 · 1994-08-17

ApplicantPlastic, Inc.
Decision Date1994-08-17
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

STYLE I WRAPPER SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Plastic, Inc.. It received FDA 510(k) clearance on 1994-08-17 under 510(k) number K943405. 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 STYLE I WRAPPER SUNGLASSES?

STYLE I WRAPPER SUNGLASSES is a medical device that received FDA 510(k) clearance on 1994-08-17. The listed applicant is Plastic, Inc.. The 510(k) number is K943405.

When did STYLE I WRAPPER SUNGLASSES receive FDA 510(k) clearance?

STYLE I WRAPPER SUNGLASSES received FDA 510(k) clearance on 1994-08-17, under 510(k) number K943405.

Who is the listed applicant for STYLE I WRAPPER SUNGLASSES?

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

What is the FDA product code for STYLE I WRAPPER SUNGLASSES?

The FDA product code for STYLE I WRAPPER 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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