FPS — Board, Bed Class I
FDA product code FPS covers "Board, Bed", a Class I medical device regulated under 21 CFR 880.6070. Submissions are reviewed by the General Hospital panel. At least 1 recent 510(k) clearance has been granted under this product code.
Classification Details
- Product Code
- FPS
- Device Class
- Class I
- Regulation Number
- 880.6070
- Submission Type
- Review Panel
- HO
- Medical Specialty
- General Hospital
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K780230 | biomet | BED BOARD | February 28, 1978 |