510(k) Report

FDA product code · General and plastic surgery

Table, Operating-Room, Ac-Powered

FQOClass I21 CFR 878.4960510(k) exempt35 decisions since 198351 recalls

FDA lists FQO 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. 35 FDA decisions since 1983. 510(k) reviews decided 2021–2025 took a median of 146 days (half between 118 and 173). 51 recalls name this code, 0 of them Class I. The most-cited predicate is K951854, named by 3 later devices.

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 FQO 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 · FQO

1in 2024

2009: 12022: 12024: 1
2007high 1 (2009) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · FQO

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

Recalls per year · FQO

8in 2024

2008: 102009: 32010: 32011: 72013: 12014: 12015: 22016: 22018: 52020: 22022: 12023: 22024: 82026 (partial year): 1
2007high 10 (2008) · low 0 (2007)2026

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

Adverse event reports per year · FQO

113in 2025

2007: 612008: 472009: 582010: 1272011: 1012012: 1202013: 1162014: 1452015: 1082016: 932017: 982018: 1042019: 1182020: 972021: 1022022: 1252023: 1872024: 1392025: 113
2007high 187 (2023) · low 47 (2008)2025

MAUDE reports naming product code FQO, 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
20070—061
20080—1047
20091—358
20100—3127
20110—7101
20120—0120
20130—1116
20140—1145
20150—2108
20160—293
20170—098
20180—5104
20190—0118
20200—297
20210—0102
20221—1125
20230—2187
20241—8139
20250—0113
20260—1—
FIG. 1 — FQO by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in FQO? 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 878.4960.