510(k) K140556
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 24, 2014
- Date Received
- March 5, 2014
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Humidifier, Respiratory Gas, (Direct Patient Interface)
- Device Class
- Class II
- Regulation Number
- 868.5450
- Review Panel
- AN
- Submission Type