Ewc: ECG II Cable Leadwire System

FDA 510(k) K984263 · Ewc

Substantially Equivalent

510(k) numberK984263

Submission

Device name
Ewc: ECG II Cable Leadwire System
Applicant
Ewc
Pewaukee, WI, US
Received
November 30, 1998
Decision date
February 2, 1999
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary 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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More from Baylis Medical Technologies, Inc.

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Questions and answers

When was Ewc: ECG II Cable Leadwire System cleared by the FDA?

Ewc: ECG II Cable Leadwire System (K984263) received a 510(k) decision of Substantially Equivalent on February 2, 1999, 64 days after the submission was received.

What is the product code of K984263?

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.