DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT— 510(k) K931922

Name: FDA 510(k) clearance K931922
Creator: U.S. Food and Drug Administration
Published: 1994-03-30

Substantially Equivalent

Viratest Intl., Inc.

FDA 510(k) clearance K931922 for DIADOT(TM) VIRUS/CHLAMYDIA TRANSPORT, Substantially Equivalent on 1994-03-30. Applicant: Viratest Intl., Inc.. Device class: 1.

Clearance details

Applicant: Viratest Intl., Inc.
Product code: Code JSM
Device class: Class 1
Regulation: 21 CFR 866.2390
Advisory panel: Microbiology
Date received: 1993-04-16
Decision date: 1994-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Antonio, TX, US

Download summary PDF View on FDA.gov ↗

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