510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935471Substantially Equivalent

Filtryzer(tm)

Toray Industries (America), Inc., Otsu-Shi, Shiga-Ken 520, JP / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935471 is the FDA 510(k) clearance record for FILTRYZER(TM), a class II device, cleared for Toray Industries (America), Inc. on under FDA product code FJI (Dialyzer, Capillary, Hollow Fiber). FDA records list 18 510(k) clearances for Toray Industries (America), Inc., from to . As of , FDA records show 2 recalls naming K935471.

Clearance record

Decision date
Received
(550 days to decision)
Product code
FJI Dialyzer, Capillary, Hollow Fiber
Regulation
21 CFR 876.5820
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Toray Industries (America), Inc. 1-1-1 Sonoyama, Otsu-Shi, Shiga-Ken 520, JP
510(k) summary
Statement
Third party review
No

Clearances, product code FJI

Trailing 12 months

FDA records hold no clearances under product code FJI in the trailing twelve months.

FDA records show no clearances under product code FJI in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code FJI, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260