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General Scanning, Inc.

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

Total Devices3
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K980565 LD2000 SERIESLMA1998-03-19 View
510(k) K973411 DIGMI-2000 (GSI INTERNAL REFERENCE)/LD2800 (MARKETING NAME)LMA1997-12-04 View
510(k) K923536 NUCLEAR MEDICINE LASER IMAGERLMC1992-11-30 View
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