FDA 510(k) FDA class 2 Substantially Equivalent 🇩🇪 Germany

CARDIO-3 CHANNEL ELECTROCARDIOGRAPH

K Number: K850454 · Decision Mar 1, 1985
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
12
Review Days
23

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Basic Information

Device Name
CARDIO-3 CHANNEL ELECTROCARDIOGRAPH
K Number
K850454
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Zimmer Elektromedizin GmbH
Date Received
February 6, 1985
Decision Date
March 1, 1985
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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