Urodynamic Instruments

FDA 510(k) K770897 · Life-Tech Instruments, Inc.

Substantially Equivalent

510(k) numberK770897

Submission

Device name
Urodynamic Instruments
Applicant
Life-Tech Instruments, Inc.
Mchenry, IL, US
Received
May 16, 1977
Decision date
June 3, 1977
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K953999Dantec Da CapoEXY · Traditional Dantec Medical, Inc.11/21/1995SE
K951442FlolabEXY · Traditional Synectics Medical, Inc.08/24/1995SE
K944972Uro-Gram Cystomrtrogram with UroflowmetryEXY · Traditional Myo/Kinetic Systems, Inc.03/08/1995SE
K9454954-CHANNEL Urodynamic Monitor with Uro-Flo OptionEXY · Traditional Fiberoptic Sensor Technlogies, Inc.02/09/1995SE
K941105Uorcap,Model Number Uds-UcapEXY · Traditional Laborie Medical Tech, Inc.05/10/1994SE
K904557MicrofloEXY · Traditional Life-Tech Intl., Inc.12/28/1990SE
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Questions and answers

When was Urodynamic Instruments cleared by the FDA?

Urodynamic Instruments (K770897) received a 510(k) decision of Substantially Equivalent on June 3, 1977, 18 days after the submission was received.

What is the product code of K770897?

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