FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

CARDIOCOLLECT PORTABLE ELECTROCARDIOGRAPH

K Number: K013367 · Decision Dec 13, 2001
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
12
Review Days
64

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Basic Information

Device Name
CARDIOCOLLECT PORTABLE ELECTROCARDIOGRAPH
K Number
K013367
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Reynolds Medical , Ltd.
Date Received
October 10, 2001
Decision Date
December 13, 2001
Product Code
DPS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DPS Electrocardiograph

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