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MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071069
510(k) Type
Traditional
Applicant
VIASYS SLEEP SYSTEMS, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2007
Days to Decision
57 days
Submission Type
Summary

MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K071069
510(k) Type
Traditional
Applicant
VIASYS SLEEP SYSTEMS, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/12/2007
Days to Decision
57 days
Submission Type
Summary