ORTHO* RUBELLA-G ANTIBODY ELISA TEST— 510(k) K896479

Substantially Equivalent

Ortho Diagnostic Systems, Inc.

FDA 510(k) clearance K896479 for ORTHO* RUBELLA-G ANTIBODY ELISA TEST, Substantially Equivalent on 1989-12-29. Applicant: Ortho Diagnostic Systems, Inc..

Clearance details

Applicant: Ortho Diagnostic Systems, Inc.
Product code: Code LFX
Advisory panel: Microbiology
Date received: 1989-11-13
Decision date: 1989-12-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carpinteria, CA, US

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