510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K851615Substantially Equivalent

Centrimed System 1 W/manual Pump Drive

Centrimed Corp., Hopkins MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K851615 is the FDA 510(k) clearance record for CENTRIMED SYSTEM 1 W/MANUAL PUMP DRIVE, a class II device, cleared for Centrimed Corp. on under FDA product code DTQ (Console, Heart-Lung Machine, Cardiopulmonary Bypass). FDA records list 4 510(k) clearances for Centrimed Corp., from to . As of , FDA records show no recalls naming K851615.

Clearance record

Decision date
Received
(61 days to decision)
Product code
DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass
Regulation
21 CFR 870.4220
Device class
Class II
Review panel
Cardiovascular
Applicant
Centrimed Corp. 651 Sixteenth Ave. S., Hopkins MN
Third party review
No

Clearances, product code DTQ

Trailing 12 months

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

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