FDA product code · Ear, nose and throat
Ultrasound Bronchoscope
5 FDA decisions since 2002. 1 recall names this code; it is not Class I. The most-cited predicate is K070983, named by 3 later devices.
An ultrasound bronchoscope is indicated for the ultrasonic visualization, diagnosis and therapeutic access to the bronchial tree or the lungs. 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 Download the data (CSV)
Twenty years of PSV 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 · PSV
2so far in 2026, the most since 2007
2026 to Oct 25, outlined.
Median 510(k) review, days · PSV
Too few PSV 510(k)s in any year since 2007 to give a median.
Recalls per year · PSV
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · PSV
1,479in 2025
MAUDE reports naming product code PSV, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 1 | — | 0 | 0 |
| 2008 | 0 | — | 0 | 0 |
| 2009 | 0 | — | 0 | 0 |
| 2010 | 0 | — | 0 | 0 |
| 2011 | 0 | — | 0 | 0 |
| 2012 | 0 | — | 0 | 0 |
| 2013 | 0 | — | 0 | 0 |
| 2014 | 0 | — | 0 | 0 |
| 2015 | 0 | — | 0 | 0 |
| 2016 | 0 | — | 0 | 16 |
| 2017 | 0 | — | 0 | 15 |
| 2018 | 0 | — | 0 | 37 |
| 2019 | 1 | — | 0 | 23 |
| 2020 | 0 | — | 0 | 149 |
| 2021 | 0 | — | 0 | 134 |
| 2022 | 0 | — | 0 | 367 |
| 2023 | 0 | — | 1 | 717 |
| 2024 | 0 | — | 0 | 627 |
| 2025 | 0 | — | 0 | 1,479 |
| 2026 | 2 | — | 0 | — |
Planning a device in PSV? 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) ReportRelated product codes
Other codes under 21 CFR 892.1550.