Sandstone Medical Technologies, LLC
FDA 510(k) medical device clearances.
Top product codes for Sandstone Medical Technologies, LLC
Recent clearances by Sandstone Medical Technologies, LLC
- K121162 — POLARIS Q-SWITCH RUBY SYSTEM
- K110897 — CORTEX CO2 / ER:YAG LASER SYSTEM
- K110502 — TRIPLEX ER. YAG / ND: YAG SYSTEM
- K110304 — APEX ER. YAG / IPL SYSTEM
- K100893 — CHEVEUX DIODE LASER SYSTEM
- K093793 — LS-40 CO2 LASER SYSTEM MODEL LS-40
- K082407 — MODIFICATION TO ULTRALIGHT II ND: YAG LASER SYSTEM
- K082101 — LS FAMILY OF CO2 LASERS WITH SCANNING HANDPIECE
- K081219 — APOLLO MINI IPL SYSTEM
- K041011 — ULTRALIGHT II ND:YAG LASER SYSTEM
- K040563 — LS FAMILY OF CO2 LASERS INCLUDING: LS-15 LASER SYSTEM (15 WATT) AND LS-25 LASER SYSTEM (25 WATT)
Data sourced from openFDA. This site is unofficial and independent of the FDA.