510(k) K203623 ยท OWB Interventional Fluoroscopic X-Ray System
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| Applicant | Philips India Limited, Pune, IN |
| Decision | Substantially Equivalent, Apr 5, 2021 |
| Received | Dec 11, 2020 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K203623
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.