510(k) K213730 ยท JOM Plethysmograph, Photoelectric, Pneumatic Or Hydraulic
MESI mTABLET TBI diagnostic system, MESI mTABLET TBI
| Applicant | Mesi, Development of Medical Devices, Ltd.; Mesi D.O.O., Ljubljana, SI |
| Decision | Substantially Equivalent, Apr 21, 2022 |
| Received | Nov 26, 2021 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K213730
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.