510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K901887Substantially Equivalent

Modified Sepacell R-Series Blood Filters

Asahi Kasei Medical MT Corp. Oita Works, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K901887 is the FDA 510(k) clearance record for MODIFIED SEPACELL R-SERIES BLOOD FILTERS, a class II device, cleared for Asahi Medical Co., Ltd. on under FDA product code CAK (Microfilter, Blood Transfusion). FDA records list 16 510(k) clearances for Asahi Kasei Medical MT Corp. Oita Works, from to . As of , FDA records show no recalls naming K901887.

Clearance record

Decision date
Received
(104 days to decision)
Product code
CAK Microfilter, Blood Transfusion
Regulation
21 CFR 880.5440
Device class
Class II
Review panel
General Hospital
Applicant
Asahi Medical Co., Ltd. Intl. Sq., Washington DC
Third party review
No

Clearances, product code CAK

Trailing 12 months

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

FDA records show no clearances under product code CAK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code CAK, 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