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

CASSETTE READER

K Number: K811253 · Decision Jul 10, 1981
Classifications
1
FEI Numbers
56
Registration Numbers
56
Same Product Code
190
Applicant Total
89
Review Days
66

Basic Information

Device Name
CASSETTE READER
K Number
K811253
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
AMERICAN EDWARDS LABORATORIES
Date Received
May 5, 1981
Decision Date
July 10, 1981
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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