FDA 510(k) Applications Submitted by MARTHA MURARI
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K100464 |
02/18/2010 |
UTASWAKO I30 (INCLUDES ACCESSORIES), UTASWAKO AFP-L3, CALIBRATOR SET, CONTROL L, CONTROL H, SAMPLE DILUTION |
WAKO CHEMICALS USA, INC. |
| K060448 |
02/21/2006 |
LUMENIS ONE FAMILY OF SYSTEMS; LUMENIS ONE. |
LUMENIS LTD. |
| K050639 |
03/14/2005 |
LUMENIS VERSACUT TISSUE MORCELLATOR SYSTEM |
LUMENIS, INC. |
| K021824 |
06/04/2002 |
DYNALINK .035 BILIARY SELF-EXPANDING STENT SYSTEM, MODELS 1010102-38,1010102-56,1010102-80,1010103-38,1010103-56, 101010 |
GUIDANT CORP. |
| K082590 |
09/08/2008 |
SYMPHONY METER REMOTE |
LIFESCAN, INC. |
| K043173 |
11/16/2004 |
Q-SWITCHED ND:YAG LASER TREATMENT HEAD FOR THE LUMENIS QUANTUM SERIES |
LUMENIS, LTD. |
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