Last synced on 14 November 2025 at 11:06 pm

MINI CPAP DEVICE AND HUMIDIFIER ACCESSORY

Page Type
Cleared 510(K)
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)
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