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

DIDECO-SHILEY AUTOTRANSFUSION ACCESSORIES

K Number: K872159 · Decision Aug 12, 1987
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
393
Applicant Total
174
Review Days
69

Basic Information

Device Name
DIDECO-SHILEY AUTOTRANSFUSION ACCESSORIES
K Number
K872159
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
SHILEY, INC.
Date Received
June 4, 1987
Decision Date
August 12, 1987
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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