Kirwan 26-2520S
by Kirwan Surgical Products LLC 3 variants
Kirwan 26-2520S is an electrosurgical system generator (FDA Class II; FDA product code GEI, Electrosurgical, Cutting & Coagulation & Accessories) made by Kirwan Surgical Products LLC, cleared under FDA 510(k) K052203 on 20 Oct 2005 and listed in FDA GUDID since 2 Nov 2022 (UDI-DI 00841019121238), active as of 23 Oct 2026.
Active
510(k)
Valid until
No expiry
FDA recalls
None found
Documents
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00841019121238 | Date2 Nov 2022 | StatusListed |
| United States | FDA 510(k)SESE | NumberK052203 | Date20 Oct 2005 | StatusActive |
Official records
- AccessGUDID record 00841019121238
- FDA 510(k) database K052203
Across registries
- FDA 510(k) K052203 decided 20 Oct 2005 Active
- FDA GUDID UDI-DI 00841019121238 listed 2 Nov 2022 Listed
Timeline
- Cleared FDA 510(k) K052203
- Listed FDA GUDID 00841019121238
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Kirwan
- Generic name
- Electrosurgical system generator
- Model / reference
- 26-2520S
- Primary DI / UDI-DI
- 00841019121238
- 510(k) Number
- FDA product code
- GEI
- GMDN term
- Electrosurgical system generator
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
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