THE DDI SERODOT RUBELLA IGG TEST KIT— 510(k) K875368

Substantially Equivalent

Disease Detection International, Inc.

FDA 510(k) clearance K875368 for THE DDI SERODOT RUBELLA IGG TEST KIT, Substantially Equivalent on 1988-03-23. Applicant: Disease Detection International, Inc..

Clearance details

Applicant: Disease Detection International, Inc.
Product code: Code LFX
Advisory panel: Microbiology
Date received: 1987-12-31
Decision date: 1988-03-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

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