Sandstone Medical Technologies, LLC
Sandstone Medical Technologies, LLC holds FDA 510(k) medical device clearances, first cleared 2004, most recent 2012.
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.