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

COMPUTER, CARDIAC OUTPUT (#SP1425)

K Number: K760532 · Decision Sep 9, 1976
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
174
Applicant Total
31
Review Days
10

Basic Information

Device Name
COMPUTER, CARDIAC OUTPUT (#SP1425)
K Number
K760532
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1435
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
GOULD, INC.
Date Received
August 30, 1976
Decision Date
September 9, 1976
Product Code
DXG
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
DXG Computer, Diagnostic, Pre-Programmed, Single-Function

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K851486 GOULD DISPOSABLE TRANSDUCER & ACCESSORIES-DTX
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