IOGYN SYSTEM— 510(k) DEN130040

Unknown

Iogyn, Inc.

FDA 510(k) clearance DEN130040 for IOGYN SYSTEM, Unknown on 2014-03-28. Applicant: Iogyn, Inc.. Device class: 2.

Clearance details

Applicant: Iogyn, Inc.
Product code: Code PGT
Device class: Class 2
Regulation: 21 CFR 884.1710
Advisory panel: Obstetrics/Gynecology
Date received: 2013-08-30
Decision date: 2014-03-28
Decision: Unknown
Clearance type: Direct
Location: Cupertino, CA, US

View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.