IN VITRO DIAGNOSTIC STANDARDS— 510(k) K802278

Substantially Equivalent

Supelco, Inc.

FDA 510(k) clearance K802278 for IN VITRO DIAGNOSTIC STANDARDS, Substantially Equivalent on 1980-11-24. Applicant: Supelco, Inc..

Clearance details

Applicant: Supelco, Inc.
Product code: Code DIF
Advisory panel: Clinical Toxicology
Date received: 1980-09-12
Decision date: 1980-11-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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