510(k) K253868

Device
QuietLab Pro
Applicant
QuietLab, LLC
510(k) number
K253868
Product code
LRK
Decision
Substantially Equivalent (SESE)
Decision date
2025-12-05
Date received
2025-12-03
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
Y

Related Records

Applicant Contact

Contact
Candriella Pietro
Address
447 Broadway 2530, 2nd Floor New York NY US 10013 10013

FDA Registration Numbers

Source Documents

510(k) summary PDF

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