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

SURFLO INJECTION PLUG

K Number: K791173 · Decision Jul 30, 1979
Classifications
1
FEI Numbers
424
Registration Numbers
424
Same Product Code
1173
Applicant Total
31
Review Days
35

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Basic Information

Device Name
SURFLO INJECTION PLUG
K Number
K791173
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Terumo America, Inc.
Date Received
June 25, 1979
Decision Date
July 30, 1979
Product Code
FPA
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
FPA Set, Administration, Intravascular

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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
K790105 TERUMO IMUGARD
K772362 AVF SET FOR SINGLE NEEDLE HEMODIALYSIS
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