FDA 510(k) FDA class 2 Substantially Equivalent 🇹🇼 Taiwan

V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER

K Number: K101569 · Decision Mar 1, 2011
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
123
Review Days
270

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Basic Information

Device Name
V-TRUST MODEL TD-2202 PORTABLE ECG RECORDER
K Number
K101569
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Taidoc Technology Corporation
Date Received
June 4, 2010
Decision Date
March 1, 2011
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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