FDA product code · General hospital
Lift, Patient, Non-Ac-Powered
FDA lists FSA as exempt from 510(k): a device of this type needs no clearance unless one of the limits in 21 CFR 880.9 applies, such as a new intended use or a different fundamental technology. 13 FDA decisions since 1978. 89 recalls name this code, 1 of them Class I.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly Download the data (CSV)
Twenty years of FSA 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 · FSA
FDA has decided no FSA device since 2007.
Median 510(k) review, days · FSA
Too few FSA 510(k)s in any year since 2007 to give a median.
Recalls per year · FSA
2in 2022
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · FSA
436in 2025
MAUDE reports naming product code FSA, 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 | 0 | — | 7 | 199 |
| 2008 | 0 | — | 19 | 235 |
| 2009 | 0 | — | 5 | 231 |
| 2010 | 0 | — | 1 | 344 |
| 2011 | 0 | — | 10 | 450 |
| 2012 | 0 | — | 4 | 981 |
| 2013 | 0 | — | 3 | 1,923 |
| 2014 | 0 | — | 0 | 1,602 |
| 2015 | 0 | — | 2 | 1,421 |
| 2016 | 0 | — | 3 | 735 |
| 2017 | 0 | — | 1 | 378 |
| 2018 | 0 | — | 3 | 367 |
| 2019 | 0 | — | 3 | 393 |
| 2020 | 0 | — | 2 (1) | 281 |
| 2021 | 0 | — | 4 | 257 |
| 2022 | 0 | — | 2 | 264 |
| 2023 | 0 | — | 0 | 342 |
| 2024 | 0 | — | 0 | 371 |
| 2025 | 0 | — | 0 | 436 |
| 2026 | 0 | — | 2 | — |
Planning a device in FSA? 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