FEATHERLITE AQUA TOCODYNAMOMETER— 510(k) K061044

Substantially Equivalent

Ventrex, Inc.

FDA 510(k) clearance K061044 for FEATHERLITE AQUA TOCODYNAMOMETER, Substantially Equivalent on 2006-07-12. Applicant: Ventrex, Inc.. Device class: 2.

Clearance details

Applicant: Ventrex, Inc.
Product code: Code HFM
Device class: Class 2
Regulation: 21 CFR 884.2720
Advisory panel: Obstetrics/Gynecology
Date received: 2006-04-14
Decision date: 2006-07-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ventura, 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.