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FDA 510(k) Applications Submitted by RONALD KOHLHARDT
FDA 510(k) Number
Submission Date
Device Name
Applicant
K011677
05/30/2001
MEDLITE Q-SWITCHED ND:YAG LASER REPLACED BY THE MEDLITE C3 Q-SWTICHED ND:YAG LASER
CONTINUUM ELECTRO-OPTICS, INC.
K013216
09/26/2001
DIODENT DENTAL LASER SYSTEM
CONTINUUM ELECTRO-OPTICS, INC.
K014234
12/26/2001
MEDLITE IV Q-SWITCHEDND: YAGLASER REPLACED BY THE MEDLITE C6 Q-SWICTHED ND: YAG LASER
CONTINUUM ELECTRO-OPTICS, INC.
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