Coaptium Connect with Tissium Light
FDA 510(k) clearance K251957 · decided 2025-09-08
Clearance details
- K-number
- K251957
- Device name
- Coaptium Connect with Tissium Light
- Applicant
- Tissium SA
- Decision
- Substantially Equivalent
- Date received
- 2025-06-25
- Decision date
- 2025-09-08
- Days to decision
- 75 days
- Clearance type
- Special
- Product code
- SFD
- Device class
- 2
- Regulation number
- 882.5270
- Medical specialty
- Neurology
- Advisory committee
- Neurology
- Location
- Paris, FR
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| COAPTIUM Connect with TISSIUM LIGHT (DEN240066) | Tissium SA | 2025-06-17 |
Recalls involving this device
No recalls on record reference this clearance.