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

D732 MICRO 27 PH.I.S.I.O. ADULT ARTERIAL FILTER

K Number: K052717 · Decision Oct 20, 2005
Classifications
1
FEI Numbers
25
Registration Numbers
25
Same Product Code
95
Applicant Total
6
Review Days
21

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Basic Information

Device Name
D732 MICRO 27 PH.I.S.I.O. ADULT ARTERIAL FILTER
K Number
K052717
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4260
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Dideco S.R.L.
Date Received
September 29, 2005
Decision Date
October 20, 2005
Product Code
DTM
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
DTM Filter, Blood, Cardiopulmonary Bypass, Arterial Line

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K Number Device Name
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K050890 ECC.O SYSTEM
K050447 PERFORMA ADULT HOLLOW FIBER MEMBRANE OXYGENATOR
K043323 D 905 EOS HOLLOW FIBER OXYGENATOR WITH INTEGRATED HARDSHELL VENOUS/CARDIOTOMY RESERVOIR
K953835 LILLIPUT 1 NEW BORN HOLLOW FIBER OXYGENATOR