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

THERMODILUTION CATHETER

K Number: K840992 · Decision May 23, 1984
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
36
Applicant Total
31
Review Days
77

Basic Information

Device Name
THERMODILUTION CATHETER
K Number
K840992
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1915
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
GOULD, INC.
Date Received
March 7, 1984
Decision Date
May 23, 1984
Product Code
KRB
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
KRB Probe, Thermodilution

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