Spes Medica Srl
Spes Medica Srl holds FDA 510(k) medical device clearances, first cleared 2009, most recent 2022.
Top product codes for Spes Medica Srl
Recent clearances by Spes Medica Srl
- K211954 — Subdural Electrode, Strip/Intraoperative Strip, Grid/Intraoperative Grid, Multi-Strip and Split Grid, Intraoperative Mapping Grid
- K212326 — AC Cream - Conductive paste
- K192606 — SAC2 - Electrode Cream
- K192603 — Spes Medica Subdermal Needle Electrodes
- K190050 — Tech Dots - Adhesive and conductive gel
- K133348 — STIM PROBE
- K120494 — DISPOSABLE ADHESIVE SURFACE ELECTRODE
- K093373 — LARYNGEAL SURFACE ELECTRODE
- K091410 — DISPOSABLE EMG NEEDLE ELECTRODES, MYOLINE, MYOLINE 2, MYOBOT,
Data sourced from openFDA. This site is unofficial and independent of the FDA.