Continuum Electro-Optics, Inc.
Continuum Electro-Optics, Inc. holds FDA 510(k) medical device clearances, first cleared 1994, most recent 2003.
Top product codes for Continuum Electro-Optics, Inc.
Recent clearances by Continuum Electro-Optics, Inc.
- K022709 — MEDLITE Q-SWITHCED LASER
- K022351 — DIODENT DENTAL LASER SYSTEM
- K021616 — DELIGHT DENTAL ER: YAG LASER SYSTEM
- K013216 — DIODENT DENTAL LASER SYSTEM
- K014234 — MEDLITE IV Q-SWITCHEDND: YAGLASER REPLACED BY THE MEDLITE C6 Q-SWICTHED ND: YAG LASER
- K011677 — MEDLITE Q-SWITCHED ND:YAG LASER REPLACED BY THE MEDLITE C3 Q-SWTICHED ND:YAG LASER
- K933057 — MULTILITE ERBIUM:YAG SURGICAL LASER SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.