FYH — Splint, Extremity, Noninflatable, External, Sterile Class I
FDA Device Classification
Classification Details
- Product Code
- FYH
- Device Class
- Class I
- Regulation Number
- 878.3910
- Submission Type
- Review Panel
- HO
- Medical Specialty
- General, Plastic Surgery
- Implant
- No
Recent 510(k) Clearances
| K-Number | Applicant | Device Name | Date |
|---|
| K925145 | trace medical equipment | TRACE MODEL #'S 840, 841, 842, 845 | May 19, 1993 |
| K924984 | johnson and johnson orthopaedics | SPECIALIST(R) WALKER | February 1, 1993 |
| K895092 | kut-guard | KUT-SHIELD | September 26, 1989 |
| K852558 | huxley instrument | SPLINTS(ALL TYPE) | July 2, 1985 |
| K843400 | compression splint products | HYDRO-SPLINT A SPONGE-COMPRESS DRESS | October 24, 1984 |
| K821693 | johnson and johnson professionals | J & J DIP WATER ADDITIVE | July 2, 1982 |
| K802522 | johnson and johnson professionals | DELTA-LITE CASTING TAPE & SPLINTS | January 8, 1981 |
| K801436 | orthopedic systems | ORTHOPEDIC LOWER EXTREMITY SUSPENSION | June 26, 1980 |