FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇳 China

PC ECG

K Number: K102854 · Decision Dec 3, 2010
Classifications
1
FEI Numbers
184
Registration Numbers
184
Same Product Code
570
Applicant Total
47
Review Days
65

Basic Information

Device Name
PC ECG
K Number
K102854
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
EDAN INSTRUMENTS, INC.
Date Received
September 29, 2010
Decision Date
December 3, 2010
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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