VIRATEST-DIA(TM) MEASLES (RUBEOLA)— 510(k) K910290

Name: FDA 510(k) clearance K910290
Creator: U.S. Food and Drug Administration
Published: 1992-03-18

Substantially Equivalent

Virus Reference Laboratory, Inc.

FDA 510(k) clearance K910290 for VIRATEST-DIA(TM) MEASLES (RUBEOLA), Substantially Equivalent on 1992-03-18. Applicant: Virus Reference Laboratory, Inc.. Device class: 1.

Clearance details

Applicant: Virus Reference Laboratory, Inc.
Product code: Code LJB
Device class: Class 1
Regulation: 21 CFR 866.3520
Advisory panel: Microbiology
Date received: 1991-01-22
Decision date: 1992-03-18
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LJB

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K974552 — DIAMEDIX IS-MEASLES IGG TEST SYSTEM1998-01-28
K971620 — QUANTA LITE RUBEOLA (MEASLES) IGG1997-07-22
K922330 — BARTELS RUBEOLA IGG EIA1992-09-02
K922335 — BARTELS RUBEOLA IGM EIA1992-09-02
K904083 — RUBEOLA IGM ELISA TEST1991-01-03

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