510(k) Report

FDA product code · Cardiovascular

Controller, Temperature, Cardiopulmonary Bypass

DWCClass II21 CFR 870.4250510(k) required30 decisions since 198121 recalls

30 FDA decisions since 1981. 510(k) reviews decided 2021–2025 took a median of 257 days (half between 256 and 257). 21 recalls name this code, 0 of them Class I. The most-cited predicate is K031544, named by 3 later devices.

If the device is reusable, validated reprocessing instructions and reprocessing validation data for this device type must be included in a 510(k) submission (82 FR 26807, available at https://www.gpo.gov/fdsys/pkg/FR-2017-06-09/pdf/2017-12007.pdf).

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026 Download the data (CSV)

FIG. A — Illustration, cardiovascular panel

Twenty years of DWC at a glance: how often FDA decides these devices, how long 510(k) reviews take, how often they are recalled, and how many adverse event reports name the code.

FDA decisions per year · DWC

2in 2022

2007: 12010: 12012: 12013: 12014: 12020: 12022: 2
2007high 2 (2022) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · DWC

Too few DWC 510(k)s in any year since 2007 to give a median.

Recalls per year · DWC

5in 2023

2010: 12012: 22014: 12015: 12016: 12017: 12018: 32021: 52023: 5
2007high 5 (2021) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · DWC

670in 2025

2007: 32009: 22010: 2432011: 2812012: 3512013: 2442014: 3782015: 5752016: 7872017: 7162018: 5642019: 6972020: 5482021: 6222022: 6052023: 9282024: 5552025: 670
2007high 928 (2023) · low 0 (2008)2025

MAUDE reports naming product code DWC, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—03
20080—00
20090—02
20101—1243
20110—0281
20121—2351
20131—0244
20141—1378
20150—1575
20160—1787
20170—1716
20180—3564
20190—0697
20201—0548
20210—5622
20222—0605
20230—5928
20240—0555
20250—0670
20260—0—
FIG. 1 — DWC by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in DWC? A 510(k) Report ranks candidate predicates in this code by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report