FDA 510(k) Applications Submitted by HARRY HAYES, PH.D

FDA 510(k) Number Submission Date Device Name Applicant
K120437 02/13/2012 TWISTER SIDE-FIRE FIBER OPTIC DELIVERY SYSTEM BIOLITEC SIA (LATVIA)
K130681 03/13/2013 ENDOVASCULAR LASER VENOUS SYSTEM KIT WITH 2 RING RADIAL EMITTING FIBER BIOLITEC SIA
K100726 03/15/2010 CERALAS D/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS E/ 980NM FIBER-COUPLED DIODE LASER FAMILY, CERALAS HPD/ 980NM BIOLITEC, INC.
K101712 06/18/2010 ENDOVASCULAR LAER VEIN SYSTEM KIT BIOLITEC, INC.
K112013 07/14/2011 EVOLVE(R) HPD 980/1470NM MULTIWAVELENGTH DIODE LASER BIOLITEC, INC.
K112253 08/05/2011 CERALAS 147NM DIODE LASER SYSTEM BIOLITEC, INC.
K112299 08/10/2011 ENDOVASCULAR LASER VEIN SYSTEM KIT BIOLITEC MEDICAL DEVICES, INC
K112324 08/12/2011 CERALAS 980NM DIODE LASER FAMILY BIOLITEC MEDICAL DEVICES, INC
K112442 08/24/2011 RADIAL-EMITTING SHAPED FIBER OPTIC DELIVERY SYSTEM BIOLITEC MEDICAL DEVICES, INC
K113688 12/15/2011 MEGABEAM REUSABLE FIBER OPTIC DELIVERY SYSTEM BIOLITEC MEDICAL DEVICES, INC
K113709 12/19/2011 MEGABEAM FIBER OPTIC DELIVERY SYSTEM WITH ADDITIONAL TIPS & HANDPIECE BIOLITEC MEDICAL DEVICES, INC
K113792 12/23/2011 MEGABEAM ENDOCULAR PROBE AND ASPIRATING ENDOCULAR PROBE BIOLITEC MEDICAL DEVICES, INC
K113858 12/30/2011 MEGABEAM ENDO-ENT PROBE BIOLITEC MEDICAL DEVICES, INC
K120231 01/25/2012 EVOLVE HPD 980/ 1470NM MULTIWAVELENGTH DIODE LASER (EVOLVE DUAL) BIOLITEC MEDICAL DEVICES, INC


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