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FDA 510(k)

REVERT SUNGLASSES & POLAR SUNGLASSES

K-Number: K953920 · 1995-09-12

ApplicantBella Occhiali, Inc.
Decision Date1995-09-12
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

REVERT SUNGLASSES & POLAR SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Bella Occhiali, Inc.. It received FDA 510(k) clearance on 1995-09-12 under 510(k) number K953920. 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 REVERT SUNGLASSES & POLAR SUNGLASSES?

REVERT SUNGLASSES & POLAR SUNGLASSES is a medical device that received FDA 510(k) clearance on 1995-09-12. The listed applicant is Bella Occhiali, Inc.. The 510(k) number is K953920.

When did REVERT SUNGLASSES & POLAR SUNGLASSES receive FDA 510(k) clearance?

REVERT SUNGLASSES & POLAR SUNGLASSES received FDA 510(k) clearance on 1995-09-12, under 510(k) number K953920.

Who is the listed applicant for REVERT SUNGLASSES & POLAR SUNGLASSES?

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

What is the FDA product code for REVERT SUNGLASSES & POLAR SUNGLASSES?

The FDA product code for REVERT SUNGLASSES & POLAR SUNGLASSES is HQY.

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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.

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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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