LNZ — Changer, Tube, Endotracheal Class II
FDA product code LNZ covers "Changer, Tube, Endotracheal", a Class II medical device regulated under 21 CFR 868.5730. Submissions are reviewed by the Anesthesiology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LNZ
- Device Class
- Class II
- Regulation Number
- 868.5730
- Submission Type
- Review Panel
- AN
- Medical Specialty
- Anesthesiology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K102127 | instrumentation industries | ENDOTRACHEAL TUBE CHANGERS | August 27, 2010 |