Minipro 8100 Urodynamic Measureing System

FDA 510(k) K910217 · Browne Medical Systems, Inc.

Substantially Equivalent

510(k) numberK910217

Submission

Device name
Minipro 8100 Urodynamic Measureing System
Applicant
Browne Medical Systems, Inc.
Minneapolis, MN, US
Received
January 17, 1991
Decision date
April 2, 1991
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FAP – Cystometric Gas (Carbon-Dioxide) On Hydraulic Device
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1620
Specialty
Gastroenterology, Urology

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K931179Urolab SpectrumFAP · Traditional Life-Tech Intl., Inc.11/18/1993SE
K922476Uro-Pro 2000FAP · Traditional Fiberoptic Sensor Technlogies, Inc.07/20/1993SE
K924383Synectics Liberty System, PC Polygraf/Polygram UroFAP · Traditional Synectics-Dantec06/18/1993SE
K923995Urodynamics Tubing Kits #5161, #5150, #7170FAP · Traditional Advanced Medical Products, Inc.04/08/1993SE
K923464Urodynamic CathetersFAP · Traditional R.L. Medical Corp.02/05/1993SE

More from R.L. Medical Corp.

510(k)DeviceDecision
K921047Model 8100 Urodynamics Measuring SystemFAP · Traditional 04/10/1992SE
K920992Profile Plus Urodynamics Measuring Syst, ModifiedFAP · Traditional 04/10/1992SE
K920991Image Pro Urodynamics Measuring Syst, ModificationFAP · Traditional 04/10/1992SE
K910444Browne Medical Systems ImageproFAP · Traditional 06/10/1991SE
K910371Urodynamic Measuring SystemFAP · Traditional 05/15/1991SE
K910285Browne Medical Syst.Inc Stand-Alone Water PumpFAP · Traditional 04/02/1991SE

Questions and answers

When was Minipro 8100 Urodynamic Measureing System cleared by the FDA?

Minipro 8100 Urodynamic Measureing System (K910217) received a 510(k) decision of Substantially Equivalent on April 2, 1991, 75 days after the submission was received.

What is the product code of K910217?

The FDA product code is FAP – Cystometric Gas (Carbon-Dioxide) On Hydraulic Device, a Class II (moderate risk) device regulated under 21 CFR 876.1620.