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

CARDIOCASSETTE II #363

K Number: K821453 · Decision May 25, 1982
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
193
Applicant Total
27
Review Days
11

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Basic Information

Device Name
CARDIOCASSETTE II #363
K Number
K821453
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Birtcher Corp.
Date Received
May 14, 1982
Decision Date
May 25, 1982
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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