RUBELLA IGG— 510(k) K902793

Substantially Equivalent

Pharmacia Diagnostics, Inc.

FDA 510(k) clearance K902793 for RUBELLA IGG, Substantially Equivalent on 1990-07-31. Applicant: Pharmacia Diagnostics, Inc.. Device class: 2.

Clearance details

Applicant: Pharmacia Diagnostics, Inc.
Product code: Code LFX
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1990-06-26
Decision date: 1990-07-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Columbia, MD, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.