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

BLOOD OXYGENATOR 50 70/S

K Number: K831895 · Decision Oct 19, 1983
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
249
Applicant Total
174
Review Days
127

Basic Information

Device Name
BLOOD OXYGENATOR 50 70/S
K Number
K831895
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4350
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
SHILEY, INC.
Date Received
June 14, 1983
Decision Date
October 19, 1983
Product Code
DTZ
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
DTZ Oxygenator, Cardiopulmonary Bypass

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