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Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172859
510(k) Type
Traditional
Applicant
Prosomnous Sleep Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2017
Days to Decision
63 days
Submission Type
Summary

Prosomnus [CA] Sleep and Snore Device and Prosomnus [CA] Sleep and Snore Device with Micro-recorder

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K172859
510(k) Type
Traditional
Applicant
Prosomnous Sleep Technologies
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/22/2017
Days to Decision
63 days
Submission Type
Summary