RUBELLA ELISA TEST SYSTEM— 510(k) K891783

Substantially Equivalent

Zeus Scientific, Inc.

FDA 510(k) clearance K891783 for RUBELLA ELISA TEST SYSTEM, Substantially Equivalent on 1989-08-03. Applicant: Zeus Scientific, Inc..

Clearance details

Applicant: Zeus Scientific, Inc.
Product code: Code LFX
Advisory panel: Microbiology
Date received: 1989-03-24
Decision date: 1989-08-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Raritan, NJ, US

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