FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OXYGENATOR GAS LINE FILTER

K Number: K792151 · Decision Nov 13, 1979
Classifications
1
FEI Numbers
48
Registration Numbers
48
Same Product Code
41
Applicant Total
9
Review Days
22

Basic Information

Device Name
OXYGENATOR GAS LINE FILTER
K Number
K792151
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4200
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
CARDIO SYSTEMS, INC.
Date Received
October 22, 1979
Decision Date
November 13, 1979
Product Code
KRI
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
KRI Accessory Equipment, Cardiopulmonary Bypass

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K921500 CENTRI-SAFE(TM) VALVE
K882177 ADD-ON TO CRITICAL PATIENT CARE BED
K852736 BAYLOR RAPID AUTOTRANSFUSION SYSTEM
K792152 CARDIOPLEGIA SOLUTION ADMIN. SET