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Isolux America

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K022384 XENON FIBEROPTIC LIGHT SOURCE, MODEL 1300 XSBPHET2002-10-18 View
510(k) K991572 ISOLUX SURGICAL HEADLIGHTFST1999-07-08 View
510(k) K991208 ENDOSCOPIC FIBEROPTIC CABLEHBI1999-06-23 View
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