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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