ORTHO RUBELLA ELISA TEST SYSTEM— 510(k) K822342

Substantially Equivalent

Ortho Diagnostic Systems, Inc.

FDA 510(k) clearance K822342 for ORTHO RUBELLA ELISA TEST SYSTEM, Substantially Equivalent on 1983-03-17. Applicant: Ortho Diagnostic Systems, Inc..

Clearance details

Applicant: Ortho Diagnostic Systems, Inc.
Product code: Code LFX
Advisory panel: Microbiology
Date received: 1982-08-04
Decision date: 1983-03-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Carpinteria, CA, US

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