Circuit Arm
Circuit Arm (91-101-US308) is a Class II device made by Corvent Medical, Inc, cleared under FDA 510(k) K241135 on 13 Nov 2024 and listed in FDA GUDID since 5 Jun 2025 (UDI-DI 00850057117219), active as of 1 Jun 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 | Number00850057117219 | Date5 Jun 2025 | StatusListed |
| United States | FDA 510(k)SESE | NumberK241135 | Date13 Nov 2024 | StatusActive |
Official records
- AccessGUDID record 00850057117219
- FDA 510(k) database K241135
Across registries
- FDA 510(k) K241135 decided 13 Nov 2024 Active
- FDA GUDID UDI-DI 00850057117219 listed 5 Jun 2025 Listed
Timeline
- Cleared FDA 510(k) K241135
- Listed FDA GUDID 00850057117219
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Generic name
- Breathing circuit tube holder
- Model / Ref / Catalog
- Circuit Arm, 91-101-US308
- Primary DI / UDI-DI
- 00850057117219
- 510(k) Number
- FDA product code
- CBK
- GMDN term
- Breathing circuit tube holder
- Device class
- Class II
- Regulation number
- 868.5895
- GUDID distribution status
- In Commercial Distribution
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