510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K233702Substantially Equivalent

SMARxT Tubing and Connectors

LivaNova USA, Inc., Arvada CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K233702 is the FDA 510(k) clearance record for SMARxT Tubing and Connectors, a class II device, cleared for LivaNova USA, Inc. on under FDA product code DWE (Tubing, Pump, Cardiopulmonary Bypass). FDA records list 49 510(k) clearances for LivaNova USA, Inc., from to . As of , FDA records show no recalls naming K233702.

Clearance record

Decision date
Received
(265 days to decision)
Product code
DWE Tubing, Pump, Cardiopulmonary Bypass
Regulation
21 CFR 870.4390
Device class
Class II
Review panel
Cardiovascular
Applicant
LivaNova USA, Inc. 14401 W. 65th Way, Arvada CO
510(k) summary
Summary PDF
Third party review
No

Clearances, product code DWE

Trailing 12 months

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

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