Fms 283551
Fms 283551 is a foot-switch (FDA Class II; FDA product code HRX, Arthroscope) made by Medos International Sàrl, cleared under FDA 510(k) K041824 on 7 Jan 2005 and listed in FDA GUDID since 1 Sep 2015 (UDI-DI 10886705016990), active as of 23 Oct 2026. 2 FDA recalls are linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number10886705016990 | Date1 Sep 2015 | StatusListed |
| United States | FDA 510(k)SESE | NumberK041824 | Date7 Jan 2005 | StatusActive |
Official records
- AccessGUDID record 10886705016990
- FDA 510(k) database K041824
Across registries
- FDA 510(k) K041824 decided 7 Jan 2005 Active
- FDA GUDID UDI-DI 10886705016990 listed 1 Sep 2015 Listed
Recalls
-
- Terminated Z-0657-2016
- Terminated Z-0656-2016
Product is incorrectly labeled. The blade configuration in the affected lots does not match the description on the label.
Timeline
- Cleared FDA 510(k) K041824
- Listed FDA GUDID 10886705016990
- Recall initiated FDA recalls Z-0657-2016
- Recall initiated FDA recalls Z-0656-2016
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Fms
- Generic name
- Foot-switch, electrical
- Model / Ref / Catalog
- 283551
- Primary DI / UDI-DI
- 10886705016990
- 510(k) Number
- FDA product code
- HRX
- GMDN term
- Foot-switch, electrical
- Device class
- Class II
- Regulation number
- 888.1100
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
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