FRIEDMANN ANALYSER 3— 510(k) K914896

Substantially Equivalent

Clement Clarke, Inc.

FDA 510(k) clearance K914896 for FRIEDMANN ANALYSER 3, Substantially Equivalent on 1992-01-23. Applicant: Clement Clarke, Inc.. Device class: 1.

Clearance details

Applicant: Clement Clarke, Inc.
Product code: Code HOK
Device class: Class 1
Regulation: 21 CFR 886.1810
Advisory panel: Ophthalmic
Date received: 1991-10-31
Decision date: 1992-01-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: England, GB

Download summary PDF View on FDA.gov ↗

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K932258 — OPTICOM M6001994-07-25
K914126 — VMX MINI-LOG FLOWMETER1993-03-05

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