510(k) Report

FDA product code · General and plastic surgery

Tourniquet, Pneumatic

KCYClass I21 CFR 878.5910510(k) exempt34 decisions since 197893 recalls

FDA lists KCY as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 878.9 applies, such as a new intended use or a different fundamental technology. 34 FDA decisions since 1978. 510(k) reviews decided 2021–2025 took a median of 233 days (half between 233 and 233). 93 recalls name this code, 0 of them Class I. The most-cited predicate is K123553, named by 1 later device.

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, general and plastic surgery panel

Twenty years of KCY 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 · KCY

1in 2021

2007: 12011: 12013: 12017: 12021: 1
2007high 1 (2007) · low 0 (2008)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KCY

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

Recalls per year · KCY

67so far in 2026, the most since 2007

2008: 72010: 32011: 12012: 12013: 12015: 22016: 12017: 22019: 22022: 12026 (partial year): 67
2007high 67 (2026) · low 0 (2007)2026

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

Adverse event reports per year · KCY

118in 2025

2007: 192008: 332009: 462010: 472011: 612012: 672013: 552014: 632015: 432016: 722017: 1102018: 1452019: 1292020: 1192021: 1302022: 902023: 3472024: 1072025: 118
2007high 347 (2023) · low 19 (2007)2025

MAUDE reports naming product code KCY, 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—019
20080—733
20090—046
20100—347
20111—161
20120—167
20131—155
20140—063
20150—243
20160—172
20171—2110
20180—0145
20190—2129
20200—0119
20211—0130
20220—190
20230—0347
20240—0107
20250—0118
20260—67—
FIG. 1 — KCY by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in KCY? 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

Related product codes

Other codes under 21 CFR 878.5910.