FDA 510(k) Applications Submitted by ISOLUX AMERICA

FDA 510(k) Number Submission Date Device Name Applicant
K022384 07/22/2002 XENON FIBEROPTIC LIGHT SOURCE, MODEL 1300 XSBP ISOLUX AMERICA
K991208 04/09/1999 ENDOSCOPIC FIBEROPTIC CABLE ISOLUX AMERICA
K991572 05/05/1999 ISOLUX SURGICAL HEADLIGHT ISOLUX AMERICA


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