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

TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1L

K Number: K850866 · Decision Apr 3, 1985
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
343
Applicant Total
43
Review Days
33

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Basic Information

Device Name
TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1L
K Number
K850866
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
876.5860
Medical Specialty
Gastroenterology, Urology
Decision
Substantially Equivalent
Applicant
Erika, Inc.
Date Received
March 1, 1985
Decision Date
April 3, 1985
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 Erika, Inc.

K Number Device Name
K853134 NATIONAL MED CARE INFUSION PUMP ADM SET #95-0001-8
K852310 NATURALYTE BICARBONATE CONCENTRATE-DRY PACK
K852309 ERIKA ART LI, 3-9621-8, 22-6, 23-4 & VEN 9714-1
K850865 TORAY INDUSTRIES FILTRYZER HOLLOW FIBER KIDNEY B1-
K850655 TORAY IND. FILTRYZER HOLLOW FIBER ARTIF. KIDNEY B2
K850654 TORAY INDUS. FILTRYZER HOLLOW FIBER ARTIFICIAL KID
K842436 ERIKA NEGATIVE PRESS. ARTERIAL BLOOD
K831175 FILTRYZER HOLLOW FIBER ARTIF. KIDNEY
K831173 TORAY INDUSTRIES FILTRYZER HOLLOW FIBER
K831176 FILTRYZER HOLLOW FIBER ARTIF. KIDNEY
Search all 43 clearances from Erika, Inc. →