510(k) K242487 ยท JAF Monitor, Ultrasonic, Nonfetal
Laminar P1 (LDH-HW-001)
| Applicant | Laminar Digital Health, Inc., Sunnyvale CA, US |
| Decision | Substantially Equivalent, Dec 13, 2024 |
| Received | Aug 21, 2024 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K242487
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.