DIAMICS CERCOL CERVICAL SAMPLE COLLECTOR SYSTEM— 510(k) K062433

Name: FDA 510(k) clearance K062433
Creator: U.S. Food and Drug Administration
Published: 2007-03-16

Substantially Equivalent

Diamics, Inc.

FDA 510(k) clearance K062433 for DIAMICS CERCOL CERVICAL SAMPLE COLLECTOR SYSTEM, Substantially Equivalent on 2007-03-16. Applicant: Diamics, Inc.. Device class: 2.

Clearance details

Applicant: Diamics, Inc.
Product code: Code HHT
Device class: Class 2
Regulation: 21 CFR 884.4530
Advisory panel: Obstetrics/Gynecology
Date received: 2006-08-21
Decision date: 2007-03-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Novato, CA, 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.