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FDA 510(k)

CCI VIDEOKERATOSCOPE/COMPARATOR

K-Number: K913022 · 1991-10-09

ApplicantCci
Decision Date1991-10-09
Product CodeHLQ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CCI VIDEOKERATOSCOPE/COMPARATOR is the device name listed in this FDA 510(k) record. The listed applicant is Cci. It received FDA 510(k) clearance on 1991-10-09 under 510(k) number K913022. 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 CCI VIDEOKERATOSCOPE/COMPARATOR?

CCI VIDEOKERATOSCOPE/COMPARATOR is a medical device that received FDA 510(k) clearance on 1991-10-09. The listed applicant is Cci. The 510(k) number is K913022.

When did CCI VIDEOKERATOSCOPE/COMPARATOR receive FDA 510(k) clearance?

CCI VIDEOKERATOSCOPE/COMPARATOR received FDA 510(k) clearance on 1991-10-09, under 510(k) number K913022.

Who is the listed applicant for CCI VIDEOKERATOSCOPE/COMPARATOR?

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

What is the FDA product code for CCI VIDEOKERATOSCOPE/COMPARATOR?

The FDA product code for CCI VIDEOKERATOSCOPE/COMPARATOR is HLQ.

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Related Devices (Code: HLQ)

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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