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

HIGH FLUX HEMODIALYSIS MEMBRANE DIALYZER OR HIGH FLUX HOLLOW FIBER DIALYZER, MODELS APS-R, -M, -S, -E, AND -EX

K Number: K041726 · Decision Jul 23, 2004
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
343
Applicant Total
16
Review Days
28

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Basic Information

Device Name
HIGH FLUX HEMODIALYSIS MEMBRANE DIALYZER OR HIGH FLUX HOLLOW FIBER DIALYZER, MODELS APS-R, -M, -S, -E, AND -EX
K Number
K041726
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Asahi Medical Co., Ltd.
Date Received
June 25, 2004
Decision Date
July 23, 2004
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

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Other Clearances by Asahi Medical Co., Ltd.

K Number Device Name
K013418 AM-BIO EXTENDED RANGE SERIES DIALYZER, MODELS WET AND DRY
K001250 APS SERIES DIALYZERS (WET MODELS), APS SERIES DIALYSIS (DRY MODELS)
K991512 ASAHI AM-R-SERIES DIALYZERS (MODIFIED), MODEL AM-NR-X
K983720 ASAHI AM-BIO SERIES DIALYZERS (WET MODELS)& (DRY MODELS), MODELS AM-BIO-50,AM-BIO-65, AM-BIO-75, AND AM-BIO-100, AM-BIO-
K970650 ASAHI AM-R SERIES DIALYZERS
K914020 MODIFIED ASAHI PAN-SERIES HEMOFILTERS
K901887 MODIFIED SEPACELL R-SERIES BLOOD FILTERS
K896976 MODIFIED SEPACELL R-500 AND R-500A BLOOD FILTERS
K896664 MODIFIED SEPACELL PL-SERIES LEUKOCYTE REMOVAL FILT
K892375 MODIFIED AM-SERIES DIALYZERS
Search all 16 clearances from Asahi Medical Co., Ltd. →