510(k) K002454
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 7, 2001
- Date Received
- August 10, 2000
- Clearance Type
- Abbreviated
- 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