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

CAPS LOW LEVEL DETECTOR & DETECTOR/BUBBLE MONITOR

K Number: K864619 · Decision Feb 3, 1987
Classifications
1
FEI Numbers
8
Registration Numbers
8
Same Product Code
13
Applicant Total
174
Review Days
71

Basic Information

Device Name
CAPS LOW LEVEL DETECTOR & DETECTOR/BUBBLE MONITOR
K Number
K864619
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4205
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
SHILEY, INC.
Date Received
November 24, 1986
Decision Date
February 3, 1987
Product Code
KRL
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
KRL Detector, Bubble, Cardiopulmonary Bypass

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