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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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