510(k) K161314
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 6, 2016
- Date Received
- May 11, 2016
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
Device Classification
- Device Name
- Humidifier, Respiratory Gas, (Direct Patient Interface)
- Device Class
- Class II
- Regulation Number
- 868.5450
- Review Panel
- AN
- Submission Type