510(k) K000405 ยท HCC Device, Biofeedback
INTERCURE LTD. RESPI-LOW
| Applicant | Intercure , Ltd., Washington DC, US |
| Decision | Substantially Equivalent, May 17, 2000 |
| Received | Feb 7, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K000405
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.