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FDA 510(k)

FRIEDMANN ANALYSER 3

K-Number: K914896 · 1992-01-23

ApplicantClement Clarke, Inc.
Decision Date1992-01-23
Product CodeHOK
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

FRIEDMANN ANALYSER 3 is the device name listed in this FDA 510(k) record. The listed applicant is Clement Clarke, Inc.. It received FDA 510(k) clearance on 1992-01-23 under 510(k) number K914896. The device is classified under product code HOK. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FRIEDMANN ANALYSER 3?

FRIEDMANN ANALYSER 3 is a medical device that received FDA 510(k) clearance on 1992-01-23. The listed applicant is Clement Clarke, Inc.. The 510(k) number is K914896.

When did FRIEDMANN ANALYSER 3 receive FDA 510(k) clearance?

FRIEDMANN ANALYSER 3 received FDA 510(k) clearance on 1992-01-23, under 510(k) number K914896.

Who is the listed applicant for FRIEDMANN ANALYSER 3?

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

What is the FDA product code for FRIEDMANN ANALYSER 3?

The FDA product code for FRIEDMANN ANALYSER 3 is HOK.

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Other records listing Clement Clarke, Inc. 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.

K961512PERKINS HAND-HELD APPLANATION TONOMETERK952713MINI WRIGHT LR AFSK953965904 SLIT LAMPK932258OPTICOM M600K914126VMX MINI-LOG FLOWMETERK912397PROFESSIONAL INDIRECT OPHTHALMOSCOPE

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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