Sydney Ivf PVP

FDA 510(k) K031304 · Cook Urological, Inc.

Substantially Equivalent

510(k) numberK031304

Submission

Device name
Sydney Ivf PVP
Applicant
Cook Urological, Inc.
Spencer, IN, US
Received
April 24, 2003
Decision date
March 23, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MQL – Media, Reproductive
Device class
Class II (moderate risk)
Regulation
21 CFR 884.6180
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Sydney Ivf PVP cleared by the FDA?

Sydney Ivf PVP (K031304) received a 510(k) decision of Substantially Equivalent on March 23, 2004, 334 days after the submission was received.

What is the product code of K031304?

The FDA product code is MQL – Media, Reproductive, a Class II (moderate risk) device regulated under 21 CFR 884.6180.