Codman® 301538
by Integra LifeSciences Production Corporation
Codman® 301538 (30-1538) is a Class II device made by Integra LifeSciences Production Corporation, cleared under FDA 510(k) K851487 on 3 May 1985 and listed in FDA GUDID since 11 May 2020 (UDI-DI 10381780513926), 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 | Number10381780513926 | Date11 May 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK851487 | Date3 May 1985 | StatusActive |
Official records
- AccessGUDID record 10381780513926
- FDA 510(k) database K851487
Across registries
- FDA 510(k) K851487 decided 3 May 1985 Active
- FDA GUDID UDI-DI 10381780513926 listed 11 May 2020 Listed
Timeline
- Cleared FDA 510(k) K851487
- Listed FDA GUDID 10381780513926
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Codman®
- Generic name
- Electrical-only medical device connection cable, single-use
- Model / Ref / Catalog
- 301538, 30-1538
- Primary DI / UDI-DI
- 10381780513926
- FDA product code
- GEI
- GMDN term
- Electrical-only medical device connection cable, single-use
- Device class
- Class II
- Regulation number
- 878.4400
- GUDID distribution status
- In Commercial Distribution
- Size
- Length — 366 CentimeterLength — 12 Feet
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