EEVATM PETRI DISH— 510(k) K103028

Substantially Equivalent

Auxogyn, Inc.

FDA 510(k) clearance K103028 for EEVATM PETRI DISH, Substantially Equivalent on 2011-08-11. Applicant: Auxogyn, Inc.. Device class: 2.

Clearance details

Applicant: Auxogyn, Inc.
Product code: Product code MQK
Device class: Class 2
Regulation: 21 CFR 884.6160
Advisory panel: Obstetrics/Gynecology
Date received: 2010-10-13
Decision date: 2011-08-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Menlo Park, 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.