510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K132166Substantially Equivalent

Venous Hardshell Cardiotomy Reservoir; Non-Coated, Non-Tight/ Vacuum-Tight/ with Softline Coating, Vacuum-Tight

MAQUET CARDIOPULMONARY GmbH, Rastatt De-Bw, DE / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K132166 is the FDA 510(k) clearance record for VENOUS HARDSHELL CARDIOTOMY RESERVOIR; NON-COATED, NON-TIGHT/ VACUUM-TIGHT/ WITH SOFTLINE COATING, VACUUM-TIGHT, a class II device, cleared for Maquet Cardiopulmonary, AG on under FDA product code DTN (Reservoir, Blood, Cardiopulmonary Bypass). FDA records list 44 510(k) clearances for Maquet Cardiopulmonary, AG, from to . As of , FDA records show no recalls naming K132166.

Clearance record

Decision date
Received
(110 days to decision)
Product code
DTN Reservoir, Blood, Cardiopulmonary Bypass
Regulation
21 CFR 870.4400
Device class
Class II
Review panel
Cardiovascular
Applicant
Maquet Cardiopulmonary, AG Kehler Strasse 31, Rastatt De-Bw, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DTN

Trailing 12 months
1 clearance under product code DTN in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DTN, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260