Echosystem
510(k) K051745
Echosystem is a medical device (FDA Class II; FDA product code LLZ, System, Image Processing, Radiological) made by Medstrat, Inc., cleared under FDA 510(k) K051745 on 14 Jul 2005, active as of 22 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 | NumberK051745 | Date14 Jul 2005 | StatusActive |
Official records
- FDA 510(k) database K051745
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA product code
- LLZ
- Device class
- Class II
- Regulation
- 21 CFR Part 892.2050
- Advisory committee
- Radiology
- FDA decision
- SESE Substantially Equivalent
Devices cleared under K051745
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 | |||
|---|---|---|---|---|
| Joints 4.0.22 | 4.0.22 | 00817886020028 | — | On the market |
| Joints 4.0.25 | 4.0.25 | 00817886020042 | — | On the market |
| Joints 5.11 | 5.11 | 00817886020240 | — | On the market |
| Joints 5.12 | 5.12 | 00817886020257 | — | On the market |
| Joints 5.14 | 5.14 | 00817886020271 | — | On the market |
| Joints 5.19 | 5.19 | 00817886020325 | — | On the market |
| Joints 5.26 | 5.26 | 00817886020394 | — | On the market |
| Joints 5.32 | 5.32 | 00817886020455 | — | On the market |
| Joints 5.37 | 5.37 | 00817886020509 | — | On the market |
| Joints 5.38 | 5.38 | 00817886020516 | — | On the market |
| Joints 6.12 | 6.12 | 00817886020677 | — | On the market |
| Joints 6.8 | 6.8 | 00817886020639 | — | On the market |
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