FDA 510(k) FDA class 2 Substantially Equivalent 🇯🇵 Japan

Asahi ViE-U Series Dialyzer

K Number: K162248 · Decision May 3, 2017
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
343
Applicant Total
5
Review Days
266

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Basic Information

Device Name
Asahi ViE-U Series Dialyzer
K Number
K162248
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Asahi Kasei Medical Co., Ltd.
Date Received
August 10, 2016
Decision Date
May 3, 2017
Product Code
KDI
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
KDI Dialyzer, High Permeability With Or Without Sealed Dialysate System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KDI), ordered by most recent decision date.

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Other Clearances by Asahi Kasei Medical Co., Ltd.

K Number Device Name
K153344 Asahi REXEED-S Series Dialyzer
K121409 ASAHI REXEED-SX/LX SERIES DIALYZER
K082515 ASAHI REXEED-SX/LX DIALYZERS, MODELS: 13SX, 15SX, 18SX, 21SX, 25SX, 13LX, 15LX, 18LX, 21LX
K051187 REXEED SERIES DIALYZERS