Salman Sinus Button
by Boston Medical Products, Inc.
510(k) K922902
Salman Sinus Button is a Class I device made by Boston Medical Products, Inc., cleared under FDA 510(k) K922902 on 18 May 1993, active as of 11 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK922902 | Date18 May 1993 | StatusActive |
Official records
- FDA 510(k) database K922902
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- KAM
- Device class
- Class I
- Regulation
- 21 CFR Part 878.4800
- Advisory committee
- General, Plastic Surgery
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K922902
Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.
| UDI-DI | Size and differences | |||
|---|---|---|---|---|
| Salman FES Stent SS2000 | SS2000 / SS2000 | 14063107102155 | — | On the market |
| Salman FES Stent SS2000 | SS2000 / SS2000 | EBESSS20000 | — | On the market |
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