FRZ — Device, Patient Transfer, Powered Class II
FDA product code FRZ covers "Device, Patient Transfer, Powered", a Class II medical device regulated under 21 CFR 880.6775. Submissions are reviewed by the General Hospital panel. At least 5 recent 510(k) clearances have been granted under this product code.
Classification Details
- Product Code
- FRZ
- Device Class
- Class II
- Regulation Number
- 880.6775
- Submission Type
- Review Panel
- HO
- Medical Specialty
- General Hospital
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|---|---|---|
| K121929 | Diacor | ZEPHYR 'X-SERIES PATIENT TRANSFER SLED | Jan 17, 2013 |
| K910830 | American Invalift | INVALIFT | Jun 9, 1992 |
| K841728 | Lehigh Consolidated Industries | LCI MEDICAL INC AIR/PAL | Jun 5, 1984 |
| K834585 | R And D Systems | CELLTRAK-B | May 2, 1984 |
| K840796 | Lancer Assoc | TENDER LIFTING CARE | Apr 20, 1984 |