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Fifth Eye, Inc.

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2022-07-14
TypeNumberDevice NameCodeDateActions
510(k) K221203 AHI SystemQNV2022-07-14 View
510(k) K212219 AHI SystemQNV2021-12-03 View
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