FDA 510(k) Applications Submitted by ROBERT KAPLAN

FDA 510(k) Number Submission Date Device Name Applicant
K855197 12/26/1985 FIBERLASE 100 ND: YAG MEDICAL LASER SYSTEM LASER MEDIA
K860063 01/06/1986 ND:YAG LASER SINGLE USE FIBER DELIVERY SYSTEM LASER MEDIA
K850509 02/08/1985 ND:YAG FIBERLASE 100 MEDICAL LASER SYSTEM LASER MEDIA
K872031 05/26/1987 UNI-FIBER NON-REPAIRABLE FIBER DELIVERY SYSTEM LASER MEDIA
K872350 06/17/1987 FIBERLASE II ND:YAG LASER FOR GASTRO.&UROLOGY USE LASER MEDIA
K872351 06/17/1987 FIBERLASE II ND:YAG LASER FOR PULMONARY USE LASER MEDIA
K872352 06/17/1987 FIBERLASE II ND:YAG LASER FOR TREAT OF MENORRHAGIA LASER MEDIA
K862444 06/26/1986 FIBERLASE 100 MEDICAL LASER SYS/ND:YAG MENORRHAGIA LASER MEDIA
K852798 07/01/1985 FIBERLASE 100 MEDICAL LASER SYSTEM LASER MEDIA
K863428 09/04/1986 SINGLE USE LASER FIBER DELIVERY SYSTEM FOR ND: YAG LASER MEDIA
K863583 09/09/1986 CHANGE IN FIBERLASE 100 ND:YAG MEDICAL LASER LASER MEDIA
K844869 12/14/1984 FIBERLASE 100 MEDICAL LASER SYSTEM LASER MEDIA
K151922 07/13/2015 StimSox(TM) System StimMed, LLC


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