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FDA 510(k)

AMITA CORPORATION VARIOUS MODELS OF SUNGLASSES

K-Number: K953744 · 1995-10-25

ApplicantAmita Corp.
Decision Date1995-10-25
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

AMITA CORPORATION VARIOUS MODELS OF SUNGLASSES is the device name listed in this FDA 510(k) record. The listed applicant is Amita Corp.. It received FDA 510(k) clearance on 1995-10-25 under 510(k) number K953744. 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 AMITA CORPORATION VARIOUS MODELS OF SUNGLASSES?

AMITA CORPORATION VARIOUS MODELS OF SUNGLASSES is a medical device that received FDA 510(k) clearance on 1995-10-25. The listed applicant is Amita Corp.. The 510(k) number is K953744.

When did AMITA CORPORATION VARIOUS MODELS OF SUNGLASSES receive FDA 510(k) clearance?

AMITA CORPORATION VARIOUS MODELS OF SUNGLASSES received FDA 510(k) clearance on 1995-10-25, under 510(k) number K953744.

Who is the listed applicant for AMITA CORPORATION VARIOUS MODELS OF SUNGLASSES?

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

What is the FDA product code for AMITA CORPORATION VARIOUS MODELS OF SUNGLASSES?

The FDA product code for AMITA CORPORATION VARIOUS MODELS OF 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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