Synectics Liberty System, PC Polygraf/Polygram Uro

FDA 510(k) K924383 · Synectics-Dantec

Substantially Equivalent

510(k) numberK924383

Submission

Device name
Synectics Liberty System, PC Polygraf/Polygram Uro
Applicant
Synectics-Dantec
Irving, TX, US
Received
August 25, 1992
Decision date
June 18, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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
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K923464Urodynamic CathetersFAP · Traditional R.L. Medical Corp.02/05/1993SE
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More from Laborie Medical Technologies, Ltd.

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K961346PH Analysis ModuleFFT · Traditional 01/29/1997SE
K925405Zinetics Composite Sensor Probe W/Internal Ref.FFT · Traditional 09/30/1994SE
K924875Microtrapper/Microdigitrapper, Add ModificationsBZQ · Traditional 06/30/1994ST
K914793Monocrystant Ph/Les Catheter, ModificationKLA · Traditional 12/13/1993SE
K913817Monocrystant Ph-Reference Catheter, ModificationFFT · Traditional 06/11/1992SE
K914624PH Meter, ModificationFFT · Traditional 04/28/1992SE
K914219Airway ThermistorBZG · Traditional 02/26/1992SE
K913387Digitrapper Mark IIIFFT · Traditional 12/27/1991SE
K904625Synectics Liberty System, PC Polygraf and PolygramBZG · Traditional 08/20/1991SE
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Questions and answers

When was Synectics Liberty System, PC Polygraf/Polygram Uro cleared by the FDA?

Synectics Liberty System, PC Polygraf/Polygram Uro (K924383) received a 510(k) decision of Substantially Equivalent on June 18, 1993, 297 days after the submission was received.

What is the product code of K924383?

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.