Biolitec Medical Devices, Inc.
Biolitec Medical Devices, Inc. holds FDA 510(k) medical device clearances, first cleared 2011, most recent 2012.
Top product codes for Biolitec Medical Devices, Inc.
Recent clearances by Biolitec Medical Devices, Inc.
- K120231 — EVOLVE HPD 980/ 1470NM MULTIWAVELENGTH DIODE LASER (EVOLVE DUAL)
- K113688 — MEGABEAM REUSABLE FIBER OPTIC DELIVERY SYSTEM
- K113858 — MEGABEAM ENDO-ENT PROBE
- K113709 — MEGABEAM FIBER OPTIC DELIVERY SYSTEM WITH ADDITIONAL TIPS & HANDPIECE
- K113792 — MEGABEAM ENDOCULAR PROBE AND ASPIRATING ENDOCULAR PROBE
- K112987 — TWISTER SIDE FIRE OPTICAL FIBER DELIVERY SYSTEM
- K112299 — ENDOVASCULAR LASER VEIN SYSTEM KIT
- K112442 — RADIAL-EMITTING SHAPED FIBER OPTIC DELIVERY SYSTEM
- K112324 — CERALAS 980NM DIODE LASER FAMILY
Data sourced from openFDA. This site is unofficial and independent of the FDA.