Corrosion Proof Dual Purpose ECG Wires

FDA 510(k) K802237 · Custom Cardio Components

Substantially Equivalent

510(k) numberK802237

Submission

Device name
Corrosion Proof Dual Purpose ECG Wires
Applicant
Custom Cardio Components
Mchenry, IL, US
Received
September 15, 1980
Decision date
October 3, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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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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More from Baylis Medical Technologies, Inc.

510(k)DeviceDecision
K802236Corrosion Proof Snap ECG Connect WiresDSA · Traditional 10/03/1980SE

Questions and answers

When was Corrosion Proof Dual Purpose ECG Wires cleared by the FDA?

Corrosion Proof Dual Purpose ECG Wires (K802237) received a 510(k) decision of Substantially Equivalent on October 3, 1980, 18 days after the submission was received.

What is the product code of K802237?

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.