510(k) K810335
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 20, 1981
- Date Received
- February 9, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Humidifier, Non-Direct Patient Interface (Home-Use)
- Device Class
- Class I
- Regulation Number
- 868.5460
- Review Panel
- AN
- Submission Type