CLEARPLAN— 510(k) K871332

Substantially Equivalent

Unipath , Ltd.

FDA 510(k) clearance K871332 for CLEARPLAN, Substantially Equivalent on 1987-08-05. Applicant: Unipath , Ltd.. Device class: 1.

Clearance details

Applicant: Unipath , Ltd.
Product code: Product code CEP
Device class: Class 1
Regulation: 21 CFR 862.1485
Advisory panel: Clinical Chemistry
Date received: 1987-04-03
Decision date: 1987-08-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Bedford Mk41 Oqg, GB

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.