LLW — Laser, Neodymium:Yag For Gynecologic Use Class II
FDA product code LLW covers "Laser, Neodymium:Yag For Gynecologic Use", a Class II medical device regulated under 21 CFR 884.4550. Submissions are reviewed by the Obstetrics/Gynecology panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- LLW
- Device Class
- Class II
- Regulation Number
- 884.4550
- Submission Type
- Review Panel
- OB
- Medical Specialty
- Obstetrics/Gynecology
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K850437 | vital signs | DISPOSABLE LARYNGOSCOPE | February 14, 1985 |