FZF — Splint, Extremity, Inflatable, External Class I
FDA Device Classification
Classification Details
- Product Code
- FZF
- Device Class
- Class I
- Regulation Number
- 878.3900
- Submission Type
- Review Panel
- SU
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
| K881516 | r. evans | COMPRESAID | April 29, 1988 |
| K874053 | vinyl technology | INFLATABLE FULL ARM SPLINT | November 23, 1987 |
| K874052 | vinyl technology | INFLATABLE HALF LEG SPLINT | November 23, 1987 |
| K874051 | vinyl technology | INFLATABLE FULL LEG SPLINT | November 23, 1987 |
| K874050 | vinyl technology | INFLATABLE FOOT & ANKLE SPLINT | November 23, 1987 |
| K853600 | hospitak | INFLATABLE AIR SPLINTS | September 19, 1985 |
| K831764 | svenol andersen | URIAS PRESSURE SPLINTS, & FIRST AID | September 12, 1983 |