510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K181954Substantially Equivalent

autoLog IQ Autotransfusion System

Medtronic Perfusion Systems, Minneapolis MN / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K181954 is the FDA 510(k) clearance record for autoLog IQ Autotransfusion System, a class II device, cleared for Medtronic Perfusion Systems on under FDA product code CAC (Apparatus, Autotransfusion). FDA records list 29 510(k) clearances for Medtronic Perfusion Systems, from to . As of , FDA records show no recalls naming K181954.

Clearance record

Decision date
Received
(30 days to decision)
Product code
CAC Apparatus, Autotransfusion
Regulation
21 CFR 868.5830
Device class
Class II
Review panel
Anesthesiology
Applicant
Medtronic Perfusion Systems 7611 Northland Dr., Minneapolis MN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code CAC

Trailing 12 months

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

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