FDA 510(k) Applications Submitted by CAROL J MORELLO, VMD

FDA 510(k) Number Submission Date Device Name Applicant
K020099 01/11/2002 MEGA BEAM/CERALAS NONSTERILE COLLIMATING HANDPIECE BIOLITEC, INC.
K010689 03/08/2001 MEGABEAM/CERALAS NON STERILE FIBER OPTIC LASER DELIVERY SYSTEMS, MODEL 200,320,400 OR 600UM BIOLITEC, INC.
K010804 03/16/2001 MEGABEAM/CERALAS REUSEABLE HANDPIECE AND DISPOSABLE TIPS BIOLITEC, INC.
K120810 03/16/2012 FIBEROPTIC LASER DELIVERY SYSTEM FIBEROPTIC FABRICATIONS INC
K991891 06/03/1999 CERALAS DIODE LASER SYSTEM, MODEL CERALAS D15 CERAMOPTEC, INC.
K001975 06/29/2000 CERALAS D10 810NM LASER, MODEL CERALAS D10-60 CERAMOPTEC, INC.
K002296 07/28/2000 CERALAS G15 532NM FREQUENCY DOUBLED ND:YAG LASER, MODEL G1-G15 CERAMOPTEC, INC.
K992773 08/18/1999 CERALAS D10 810NM DIODE LASER CERAMOPTEC, INC.
K993002 09/07/1999 CERALAS D 980NM DIODE LASER SYSTEM, MODEL D15 CERAMOPTEC, INC.
K013193 09/24/2001 MEGA BEAM/CERALAS NONSTERILE COLLIMATING HANDPIECE BIOLITEC, INC.
K954834 10/20/1995 CERALAS G FREQUENCY DOUBLED ND;YAG LASER SYSTEM CERAMOPTEC, INC.
K993828 11/12/1999 CERALAS D10 810NM DIODE LASER CERAMOPTEC, INC.
K993911 11/16/1999 CERALAS D DIODE LASER SYSTEM, MODEL D15, D25,D50 CERAMOPTEC, INC.
K962948 07/29/1996 CERALAS G ND;YAG LASER SYSTEM (CERALAS G) CERAMOPTEC, INC.


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