510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
Medical Device
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K112229Substantially Equivalent

Sarn Centrifugal Pump

Terumo Cardiovascular Systems Corporation, Ann Arbor MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K112229 is the FDA 510(k) clearance record for SARN CENTRIFUGAL PUMP, a class II device, cleared for Terumo Cardiovascular Systems on under FDA product code KFM (Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type). FDA records list 160 510(k) clearances for Terumo Cardiovascular Systems, from to . As of , FDA records show 4 recalls naming K112229.

Clearance record

Decision date
Received
(128 days to decision)
Product code
KFM Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type
Regulation
21 CFR 870.4360
Device class
Class II
Review panel
Cardiovascular
Applicant
Terumo Cardiovascular Systems 6200 Jackson Rd., Ann Arbor MI
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KFM

Trailing 12 months

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

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