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Tinnitus Control, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K061111 TINNITUS PHASE-OUTKLW2006-05-16 View
510(k) K031624 TINNITUS RXKLW2003-07-24 View
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