AMPLICOR CT/NG TEST FOR CHLAMYDIA TRACHOMATIS; ROCHE SCRIPTS FOR CT/NG TEST ACCESSORY— 510(k) K070174

Name: FDA 510(k) clearance K070174
Creator: U.S. Food and Drug Administration
Published: 2007-04-16

Substantially Equivalent

Roche Diagnostics Corporation

FDA 510(k) clearance K070174 for AMPLICOR CT/NG TEST FOR CHLAMYDIA TRACHOMATIS; ROCHE SCRIPTS FOR CT/NG TEST ACCESSORY, Substantially Equivalent on 2007-04-16. Applicant: Roche Diagnostics Corporation. Device class: 1.

Clearance details

Applicant: Roche Diagnostics Corporation
Product code: Code MKZ
Device class: Class 1
Regulation: 21 CFR 866.3120
Advisory panel: Microbiology
Date received: 2007-01-18
Decision date: 2007-04-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

Download summary PDF View on FDA.gov ↗

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