FDA product code · Radiology

Radiology-Diagnostic Kit

Name: FDA decisions, review times, recalls and adverse event reports for product code OIP
Creator: 510(k) Report

OIPClass II21 CFR 892.1680510(k) exempt0 decisions5 recalls

FDA lists OIP as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 892.9 applies, such as a new intended use or a different fundamental technology. 0 FDA decisions. 5 recalls name this code, 0 of them Class I.

FDA has exempted these devices from the premarket notification requirement by publishing in the Federal Register of July 11, 2017 (82 FR 31976) available at https://www.federalregister.gov/documents/2017/07/11/2017-14453/medical-devices-exemptions-from-premarket-notification-class-ii-devices subject to the limitations under 21 CFR XXX.9, where XXX refers to Parts 862-892, and any limitations on the exemption…

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, radiology panel

Twenty years of OIP 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 · OIP

FDA has decided no OIP device since 2007.

Median 510(k) review, days · OIP

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

Recalls per year · OIP

1in 2025

2007high 2 (2021) · low 0 (2007)2026

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

Adverse event reports per year · OIP

1in 2023

2007high 2 (2021) · low 0 (2007)2025

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

View these four charts as a table

Year	Median 510(k) review, days	Recalls (Class I)	MAUDE reports
2007	—	0	0
2008	—	0	0
2009	—	0	0
2010	—	0	0
2011	—	0	0
2012	—	0	0
2013	—	0	0
2014	—	0	0
2015	—	0	0
2016	—	0	0
2017	—	0	0
2018	—	0	1
2019	—	0	0
2020	—	0	0
2021	—	2	2
2022	—	1	0
2023	—	1	1
2024	—	0	0
2025	—	1	0
2026	—	0	—

FIG. 1 — OIP by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports, MAUDE · Data through Oct 25, 2026

Planning a device in OIP? 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 892.1680.

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Radiology-Diagnostic Kit

What has been recalled in OIP lately?

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