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

CARDIOPLEGIA SOLUTION ADMIN. SET

K Number: K792152 · Decision Nov 13, 1979
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
400
Applicant Total
9
Review Days
22

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Basic Information

Device Name
CARDIOPLEGIA SOLUTION ADMIN. SET
K Number
K792152
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Cardio Systems, Inc.
Date Received
October 22, 1979
Decision Date
November 13, 1979
Product Code
DWF
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
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

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