MODIFIED ACCUFLUOR PHENOBARBITAL REAGENT & CALIBRA— 510(k) K900704

Substantially Equivalent

Innotron of Oregon, Inc.

FDA 510(k) clearance K900704 for MODIFIED ACCUFLUOR PHENOBARBITAL REAGENT & CALIBRA, Substantially Equivalent on 1990-04-12. Applicant: Innotron of Oregon, Inc..

Clearance details

Applicant: Innotron of Oregon, Inc.
Product code: Code LGQ
Advisory panel: Clinical Toxicology
Date received: 1990-02-12
Decision date: 1990-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Portland, OR, US

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