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FDA 510(k) Applications Submitted by Mike Lee
FDA 510(k) Number
Submission Date
Device Name
Applicant
K250482
02/19/2025
Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue
Fissiontech LLC
K233850
12/05/2023
Difiney Anti Snoring Device
Fissiontech LLC
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