Biolitec Medical Devices, Inc.
FDA 510(k) medical device clearances.
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.