510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K915363Substantially Equivalent

Sarns 7850 Centrifugal Pump (Modified)

3M Company, Ann Arbor MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K915363 is the FDA 510(k) clearance record for SARNS 7850 CENTRIFUGAL PUMP (MODIFIED), a class II device, cleared for 3M Health Care, Ltd. on under FDA product code KFM (Pump, Blood, Cardiopulmonary Bypass, Non-Roller Type). FDA records list 58 510(k) clearances for 3M COMPANY, from to . As of , FDA records show one recall naming K915363.

Clearance record

Decision date
Received
(609 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
3M Health Care, Ltd. 6200 Jackson Rd., Ann Arbor MI
510(k) summary
Summary
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