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

FULL-DISCLOSURE AMBULATORY ECG SYSTEM

K Number: K823529 · Decision Dec 15, 1982
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
36
Review Days
22

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Basic Information

Device Name
FULL-DISCLOSURE AMBULATORY ECG SYSTEM
K Number
K823529
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Clinical Data, Inc.
Date Received
November 23, 1982
Decision Date
December 15, 1982
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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