Procath Pacing Threshold Cable

FDA 510(k) K941058 · Professional Catheter Corp.

Substantially Equivalent

510(k) numberK941058

Submission

Device name
Procath Pacing Threshold Cable
Applicant
Professional Catheter Corp.
Berlin, NJ, US
Received
March 8, 1994
Decision date
July 11, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DSA – Cable, Transducer And Electrode, Patient, (Including Connector)
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2900
Specialty
Cardiovascular

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K243545Philips Reusable ECG Lead Sets and Trunk Cables : Model Number,Model Name: 989803170171…DSA · Traditional Philips Medizin Systeme Böblingen GmbH01/17/2025SE
K240087RT Carbon ECG LeadsDSA · Traditional Ivy Biomedical Systems, Inc.09/13/2024SE
K240377LIFEPAK® ECG CablesDSA · Traditional Stryker Physio-Control05/07/2024SE
K240156LIFEPAK® Invasive Pressure Adapter Cable (Interfaces with ICU Medical Transpack IV…DSA · Traditional Physio-Control, Inc.04/30/2024SE
K222712Fogg System Patient Monitoring CablesDSA · Traditional Fogg System Company, Inc.11/22/2023SE
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Questions and answers

When was Procath Pacing Threshold Cable cleared by the FDA?

Procath Pacing Threshold Cable (K941058) received a 510(k) decision of Substantially Equivalent on July 11, 1994, 125 days after the submission was received.

What is the product code of K941058?

The FDA product code is DSA – Cable, Transducer And Electrode, Patient, (Including Connector), a Class II (moderate risk) device regulated under 21 CFR 870.2900.