FDA 510(k) Applications Submitted by Isabella Carrer
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K100558 |
03/01/2010 |
QUANTA DIODE LASER SYSTEM |
QUANTA SYSTEM, S.P.A. |
K090962 |
04/06/2009 |
CYBER SURGICAL LASER FAMILY INCLUDING: CYBER TM, CYBER GREEN, CYBER GREEN TM |
QUANTA SYSTEM, S.P.A. |
K091909 |
06/25/2009 |
LITHO LASER SYSTEM |
QUANTA SYSTEM, S.P.A. |
K072034 |
07/25/2007 |
DIODE MEDICAL LASER FAMILY, MODELS 4, 6, 30 |
QUANTA SYSTEM, S.P.A. |
K102749 |
09/23/2010 |
QUANTA CYBER TM 150W |
Quanta System SpA |
K083207 |
10/31/2008 |
ULTRAWAVE III EX 1320 |
QUANTA SYSTEM, S.P.A. |
K103539 |
12/02/2010 |
QUANTA SYSTEM DUOLITE |
QUANTA SYSTEM, S.P.A. |
K083613 |
12/08/2008 |
QUANTA SYSTEM POLYSURGE DIODE LASER FAMILY |
QUANTA SYSTEM, S.P.A. |
K163449 |
12/08/2016 |
HyPHo Laser System |
Hyper Photonics SRL |
K073549 |
12/18/2007 |
Q-PLUS T |
QUANTA SYSTEM, S.P.A. |
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