510(k) K172655 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
Automated ankle brachial pressure index measuring device
| Applicant | Mesi D.O.O.; Mesi, Development of Medical Devices, Ltd., Ljubljana, SI |
| Decision | Substantially Equivalent, Jan 11, 2018 |
| Received | Sep 5, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K172655
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.