RUBELLA-CUBE(TM)— 510(k) K892051

Substantially Equivalent

Difco Laboratories, Inc.

FDA 510(k) clearance K892051 for RUBELLA-CUBE(TM), Substantially Equivalent on 1989-06-08. Applicant: Difco Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Difco Laboratories, Inc.
Product code: Code LFX
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1989-03-29
Decision date: 1989-06-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Detroit, MI, US

Download summary PDF View on FDA.gov ↗

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