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

BLOOD FILTER, MICROEMBOLI-ATS-F10

K Number: K780145 · Decision Feb 2, 1978
Classifications
1
FEI Numbers
14
Registration Numbers
14
Same Product Code
35
Applicant Total
69
Review Days
3

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Basic Information

Device Name
BLOOD FILTER, MICROEMBOLI-ATS-F10
K Number
K780145
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Sorensen Research
Date Received
January 30, 1978
Decision Date
February 2, 1978
Product Code
CAK
Advisory Committee
General Hospital
Review Advisory Committee
HO
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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K833096 TRANSDUCER DOME DS106
K832957 FLOW-DIRECTED HEPARIN COATED THERMODIL
K831506 DISP. TRANSDUCER W/MONITORING KIT TRANS
K831939 TALL FLOOR STAND TFS-01
K831505 THORACIC GAUGE #TG-60 -VACUUM REGULATOR
K820706 WATERLESS SEAL & VACUUM REGULATOR
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