RUBELLA IGG ELISA TEST— 510(k) K915893

Substantially Equivalent

Gull Laboratories, Inc.

FDA 510(k) clearance K915893 for RUBELLA IGG ELISA TEST, Substantially Equivalent on 1992-03-04. Applicant: Gull Laboratories, Inc.. Device class: 2.

Clearance details

Applicant: Gull Laboratories, Inc.
Product code: Code LFX
Device class: Class 2
Regulation: 21 CFR 866.3510
Advisory panel: Microbiology
Date received: 1991-12-24
Decision date: 1992-03-04
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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