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Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250482
510(k) Type
Traditional
Applicant
Fissiontech, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2025
Days to Decision
78 days
Submission Type
Summary

Advanced Anti Snoring Device 4.0 Clear/ Advanced Anti Snoring Device 4.0 Blue

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K250482
510(k) Type
Traditional
Applicant
Fissiontech, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/8/2025
Days to Decision
78 days
Submission Type
Summary