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

CLIRANS TE15 HOLLOW FIBER DIALYZER

K Number: K801193 · Decision Aug 12, 1980
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
112
Applicant Total
31
Review Days
85

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Basic Information

Device Name
CLIRANS TE15 HOLLOW FIBER DIALYZER
K Number
K801193
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5630
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Terumo America, Inc.
Date Received
May 19, 1980
Decision Date
August 12, 1980
Product Code
KDJ
Advisory Committee
Gastroenterology, Urology
Review Advisory Committee
GU
Third Party
N

Classifications

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

Product Code Device Name
KDJ Set, Administration, For Peritoneal Dialysis, Disposable

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Other Clearances by Terumo America, Inc.

K Number Device Name
K811523 PLASMA FLEX
K802970 TERUMO HOLLOW FIBER OXYGENATOR
K802441 CLIRANS TH10 HOLLOW FIBER DIALYZER
K802122 CLIRANS TH13 HOLLOW FIBER DIALYZER
K801192 CLIRANS TE10 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
Search all 31 clearances from Terumo America, Inc. →