THE APTUS (AUTOMATED) APPLICATION OF THE RUBELLA IGM ELISA TEST SYSTEM— 510(k) K984180

Substantially Equivalent

Zeus Scientific, Inc.

FDA 510(k) clearance K984180 for THE APTUS (AUTOMATED) APPLICATION OF THE RUBELLA IGM ELISA TEST SYSTEM, Substantially Equivalent on 1999-07-20. Applicant: Zeus Scientific, Inc..

Clearance details

Applicant: Zeus Scientific, Inc.
Product code: Code LFX
Advisory panel: Microbiology
Date received: 1998-11-23
Decision date: 1999-07-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Branchburg, NJ, US

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