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

TERUFUSION BLOOD ADMIN. SET

K Number: K771209 · Decision Jul 26, 1977
Classifications
1
FEI Numbers
440
Registration Numbers
440
Same Product Code
687
Applicant Total
31
Review Days
21

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Basic Information

Device Name
TERUFUSION BLOOD ADMIN. SET
K Number
K771209
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5570
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Terumo America, Inc.
Date Received
July 5, 1977
Decision Date
July 26, 1977
Product Code
FMI
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
FMI Needle, Hypodermic, Single Lumen

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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
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