FDA 510(k) Applications Submitted by FISMA, INC.

FDA 510(k) Number Submission Date Device Name Applicant
K000158 01/19/2000 VEINLASE, MODEL E50-K8-B5, SPECTRUM K8, MODEL E50-K8-B9 FISMA, INC.
K963124 08/12/1996 PC LASER WITH SMART PLUG (PC EDO & DENTAL 200) FISMA, INC.
K990174 01/19/1999 ATLAS-ELITE,MODEL E-80,CORIUM 200,CORIUM 400, MODEL E-90, ELITE, MODEL E-80-II, ELITE ULTRA, MODEL E-80-IV FISMA, INC.
K991464 04/27/1999 DENTAL 200, DENTAL 300, DENTAL 400, MODELS E-20, E-60, E-50 FISMA, INC.


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