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

PLASMA FLEX

K Number: K811523 · Decision Sep 9, 1981
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
15
Applicant Total
31
Review Days
103

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Basic Information

Device Name
PLASMA FLEX
K Number
K811523
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.9100
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Terumo America, Inc.
Date Received
May 29, 1981
Decision Date
September 9, 1981
Product Code
KSR
Advisory Committee
Hematology
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
KSR Container, Empty, For Collection & Processing Of Blood & Blood Components

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K802970 TERUMO HOLLOW FIBER OXYGENATOR
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K801192 CLIRANS TE10 HOLLOW FIBER DIALYZER
K801193 CLIRANS TE15 HOLLOW FIBER DIALYZER
K801194 CLIRANS TE07 HOLLOW FIBER DIALYZER
K791411 COAXIAL DUAL FLOW CATHETER
K791173 SURFLO INJECTION PLUG
K790105 TERUMO IMUGARD
K772362 AVF SET FOR SINGLE NEEDLE HEMODIALYSIS
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