510(k) K233850

Device
Difiney Anti Snoring Device
Applicant
Fissiontech, LLC
510(k) number
K233850
Product code
LRK
Decision
Substantially Equivalent (SESE)
Decision date
2024-04-18
Date received
2023-12-05
Regulation
872.5570
Classification name
Device, Anti-Snoring
Medical specialty
Dental
Review panel
Dental
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Mike Lee
Address
1 Liberty St., Floor 3 New York NY US 10006 10006

FDA Registration Numbers

Source Documents

510(k) summary PDF

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