FRZ — Device, Patient Transfer, Powered Class II
FDA Device Classification
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 | January 17, 2013 |
| K910830 | american invalift | INVALIFT | June 9, 1992 |
| K841728 | lehigh consolidated industries | LCI MEDICAL INC AIR/PAL | June 5, 1984 |
| K834585 | r and d systems | CELLTRAK-B | May 2, 1984 |
| K840796 | lancer assoc | TENDER LIFTING CARE | April 20, 1984 |