510(k) K925040 ยท JEH Plethysmograph, Volume
TELEPULSE
| Applicant | Biometrix , Ltd., Greenwich CT, US |
| Decision | Substantially Equivalent, Aug 23, 1993 |
| Received | Oct 5, 1992 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K925040
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.