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

PORTABLE, ELECTROCARDIOGRAPH (ECG) MONITOR, MODEL HCG-801

K Number: K060766 · Decision Jun 9, 2006
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
570
Applicant Total
54
Review Days
79

Basic Information

Device Name
PORTABLE, ELECTROCARDIOGRAPH (ECG) MONITOR, MODEL HCG-801
K Number
K060766
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
OMRON HEALTHCARE, INC.
Date Received
March 22, 2006
Decision Date
June 9, 2006
Product Code
DPS
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

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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