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Zyppah Anti-Snoring Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182312
510(k) Type
Traditional
Applicant
Always More Marketing
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2019
Days to Decision
150 days
Submission Type
Summary

Zyppah Anti-Snoring Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K182312
510(k) Type
Traditional
Applicant
Always More Marketing
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/24/2019
Days to Decision
150 days
Submission Type
Summary