ASO-CUBE(TM)— 510(k) K901371

Substantially Equivalent

Difco Laboratories, Inc.

FDA 510(k) clearance K901371 for ASO-CUBE(TM), Substantially Equivalent on 1990-05-15. Applicant: Difco Laboratories, Inc.. Device class: 1.

Clearance details

Applicant: Difco Laboratories, Inc.
Product code: Code GTQ
Device class: Class 1
Regulation: 21 CFR 866.3720
Advisory panel: Microbiology
Date received: 1990-03-23
Decision date: 1990-05-15
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Detroit, MI, US

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