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

H12+HOLTER RECORDER

K Number: K021373 · Decision Jun 27, 2002
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
59
Applicant Total
51
Review Days
57

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Basic Information

Device Name
H12+HOLTER RECORDER
K Number
K021373
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mortara Instrument, Inc.
Date Received
May 1, 2002
Decision Date
June 27, 2002
Product Code
MWJ
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
MWJ Electrocardiograph, Ambulatory (Without Analysis)

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K152626 H3+ Holter Recorder
K152944 Xscribe Stress Exercise Testing Systems, Q-Stress Stress Exercise Testing Systems
K141020 SURVEYOR S4 MOBILE MONITOR
K133989 AMBULO 2400 AMBULATORY BLOOD PRESSURE MONITORING SYSTEM
K141811 MORTARA MONITORING WAVEFORM VIEWER
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