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

PHILIPS TRACEMASTER ECG MANAGEMENT SYSTEM, MODELS M5100A AND M5101A

K Number: K032103 · Decision Jul 22, 2003
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
107
Review Days
14

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Basic Information

Device Name
PHILIPS TRACEMASTER ECG MANAGEMENT SYSTEM, MODELS M5100A AND M5101A
K Number
K032103
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Philips Medical Systems
Date Received
July 8, 2003
Decision Date
July 22, 2003
Product Code
DSH
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
DSH Recorder, Magnetic Tape, Medical

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