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

CARDIOCASSETTE II, AMBULATORY ECG SYSTEM

K Number: K790509 · Decision Mar 23, 1979
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
13
Review Days
8

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Basic Information

Device Name
CARDIOCASSETTE II, AMBULATORY ECG SYSTEM
K Number
K790509
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Cambridge Instruments, Inc.
Date Received
March 15, 1979
Decision Date
March 23, 1979
Product Code
DSH
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
DSH Recorder, Magnetic Tape, Medical

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