510(k) Report

FDA product code · General hospital

Closed Antineoplastic And Hazardous Drug Reconstitution And Transfer System

ONBClass II21 CFR 880.5440510(k) required41 decisions since 201350 recalls

41 FDA decisions since 2013. 510(k) reviews decided 2021–2025 took a median of 115 days (half between 67 and 268). 50 recalls name this code, 1 of them Class I. The most-cited predicate is K123213, named by 9 later devices.

Reconstitute and transfer antineoplastic and other hazardous drugs in healthcare setting indicated to reduce exposure of healthcare personnel to chemotherapy agents in healthcare setting.

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 hospital panel

Twenty years of ONB 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 · ONB

6in 2025

2013: 32014: 22015: 32017: 22018: 62019: 12020: 32021: 32022: 12023: 32024: 82025: 6
2007high 8 (2024) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · ONB

60in 2025

2013: 58 days median2015: 235 days median2018: 249 days median2020: 213 days median2021: 277 days median2023: 175 days median2024: 102 days median2025: 60 days median
2007high 277 (2021) · low 58 (2013)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · ONB

38in 2025

2016: 12019: 1, 1 Class I2020: 42022: 12023: 12024: 12025: 382026 (partial year): 3
2007high 38 (2025) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · ONB

934in 2025

2012: 12013: 22014: 32015: 42016: 132017: 662018: 2282019: 4642020: 4422021: 5482022: 4482023: 4562024: 6862025: 934
2007high 934 (2025) · low 0 (2007)2025

MAUDE reports naming product code ONB, 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—00
20080—00
20090—00
20100—00
20110—00
20120—01
201335802
20142—03
2015323504
20160—113
20172—066
201862490228
20191—1 (1)464
202032134442
202132770548
20221—1448
202331751456
202481021686
202566038934
20260—3—
FIG. 1 — ONB by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in ONB? 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 880.5440.