B.Braun Melsungen AG
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories2
Latest FDA decision2017-04-28
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K163358 | Introcan Safety 3 Closed IV Catheter | FOZ | 2017-04-28 | View |
| 510(k) | K152050 | Pencylcap | FMI | 2016-03-02 | View |
No matching devices.
Related Clinical Trials
NCT02460042Clinical Post Market Clinical Follow-up (PMCF) on Peripheral Arteries Treated With SeQuent® Please Over The Wire (OTW)COMPLETEDNCT04470934SeQuent® SCB "All Comers" Post Market Clinical Follow-up (PMCF)ACTIVE_NOT_RECRUITINGNCT07363161BASel Kosten-Effektivitäts-Trial: Drug-coated BALLoon (DCB) vs. Drug-eluting Stent (DES) Strategy in High-risk Patients With Coronary Artery Disease (CAD)RECRUITING