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

ULTIPOR SQ40S BLOOD TRANSFUSION FILTER

K Number: K811985 · Decision Jul 28, 1981
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
35
Applicant Total
28
Review Days
15

Basic Information

Device Name
ULTIPOR SQ40S BLOOD TRANSFUSION FILTER
K Number
K811985
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
PALL BIOMEDICAL PRODUCTS CO.
Date Received
July 13, 1981
Decision Date
July 28, 1981
Product Code
CAK
Advisory Committee
General Hospital
Review Advisory Committee
HE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
CAK Microfilter, Blood Transfusion

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