510(k) K231666 ยท ITX Transducer, Ultrasonic, Diagnostic
Endoscopic Ultrasonic Probe (P2612S-L); Endoscopic Ultrasonic Probe (P2620S-L)
| Applicant | FUJIFILM Healthcare Americas Corporation, Lexington MA, US |
| Decision | Substantially Equivalent, Dec 13, 2023 |
| Received | Jun 7, 2023 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K231666
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.