510(k) K013241
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 21, 2002
- Date Received
- September 28, 2001
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Needle, Emergency Airway
- Device Class
- Class II
- Regulation Number
- 868.5090
- Review Panel
- AN
- Submission Type