INTRAUTERINE INSEMINATION (IUI) CATHETER— 510(k) K120154

Substantially Equivalent

Catheter Research, Inc.

FDA 510(k) clearance K120154 for INTRAUTERINE INSEMINATION (IUI) CATHETER, Substantially Equivalent on 2012-03-21. Applicant: Catheter Research, Inc..

Clearance details

Applicant: Catheter Research, Inc.
Product code: Code MQF
Advisory panel: Obstetrics/Gynecology
Date received: 2012-01-18
Decision date: 2012-03-21
Decision: Substantially Equivalent
Clearance type: Abbreviated
Location: Indianapolis, IN, US

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