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FDA 510(k)

LEVIGATOR, KEELER PHOKO

K-Number: K782141 · 1979-01-26

ApplicantKeeler Optical Products , Ltd.
Decision Date1979-01-26
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LEVIGATOR, KEELER PHOKO is the device name listed in this FDA 510(k) record. The listed applicant is Keeler Optical Products , Ltd.. It received FDA 510(k) clearance on 1979-01-26 under 510(k) number K782141. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEVIGATOR, KEELER PHOKO?

LEVIGATOR, KEELER PHOKO is a medical device that received FDA 510(k) clearance on 1979-01-26. The listed applicant is Keeler Optical Products , Ltd.. The 510(k) number is K782141.

When did LEVIGATOR, KEELER PHOKO receive FDA 510(k) clearance?

LEVIGATOR, KEELER PHOKO received FDA 510(k) clearance on 1979-01-26, under 510(k) number K782141.

Who is the listed applicant for LEVIGATOR, KEELER PHOKO?

The FDA 510(k) record lists Keeler Optical Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LEVIGATOR, KEELER PHOKO?

The FDA product code for LEVIGATOR, KEELER PHOKO is HQC.

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Other records listing Keeler Optical Products , Ltd. 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.

K810403KEELER/KONAN SPECULAR MICROSCOPEK801418KEELER AMOILS ACULL CRYO OPHTHALMIC UNITK792255NEVYAS AUTOPRESS EYE COMPRESSORK781892LOCATOR, FOREIGN BODY

Related Devices (Code: HQC)

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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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