510(k) K203231 ยท LDD Dc-Defibrillator, Low-Energy, (Including Paddles)
Switched Internal Paddles
| Applicant | Philips North America, LLC, Bothell WA, US |
| Decision | Substantially Equivalent, Jan 11, 2021 |
| Received | Nov 2, 2020 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K203231
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.