Uro-Gram Cystomrtrogram with Uroflowmetry

FDA 510(k) K944972 · Myo/Kinetic Systems, Inc.

Substantially Equivalent

510(k) numberK944972

Submission

Device name
Uro-Gram Cystomrtrogram with Uroflowmetry
Applicant
Myo/Kinetic Systems, Inc.
Menomonee Falls, WI, US
Received
October 11, 1994
Decision date
March 8, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
EXY – Uroflowmeter
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1800
Specialty
Gastroenterology, Urology

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K932764Therapeutic Stimulator 300(TS-300) & 300P(TS-300P)IPF · Traditional 10/01/1993SE
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Questions and answers

When was Uro-Gram Cystomrtrogram with Uroflowmetry cleared by the FDA?

Uro-Gram Cystomrtrogram with Uroflowmetry (K944972) received a 510(k) decision of Substantially Equivalent on March 8, 1995, 148 days after the submission was received.

What is the product code of K944972?

The FDA product code is EXY – Uroflowmeter, a Class II (moderate risk) device regulated under 21 CFR 876.1800.