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FDA 510(k)

CLAS PHOTOKERATOSCOPE

K-Number: K895741 · 1990-07-11

ApplicantKera-Metrics Corp.
Decision Date1990-07-11
Product CodeHLQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CLAS PHOTOKERATOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Kera-Metrics Corp.. It received FDA 510(k) clearance on 1990-07-11 under 510(k) number K895741. The device is classified under product code HLQ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CLAS PHOTOKERATOSCOPE?

CLAS PHOTOKERATOSCOPE is a medical device that received FDA 510(k) clearance on 1990-07-11. The listed applicant is Kera-Metrics Corp.. The 510(k) number is K895741.

When did CLAS PHOTOKERATOSCOPE receive FDA 510(k) clearance?

CLAS PHOTOKERATOSCOPE received FDA 510(k) clearance on 1990-07-11, under 510(k) number K895741.

Who is the listed applicant for CLAS PHOTOKERATOSCOPE?

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

What is the FDA product code for CLAS PHOTOKERATOSCOPE?

The FDA product code for CLAS PHOTOKERATOSCOPE is HLQ.

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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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