Codman Microsensor® 826633
by Integra LifeSciences Production Corporation
Codman Microsensor® 826633 (82-6633) is a Class II device made by Integra LifeSciences Production Corporation, cleared under FDA 510(k) K991222 on 9 Jul 1999 and listed in FDA GUDID since 1 Apr 2020 (UDI-DI 10381780520436), 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 | Number10381780520436 | Date1 Apr 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK991222 | Date9 Jul 1999 | StatusActive |
Official records
- AccessGUDID record 10381780520436
- FDA 510(k) database K991222
Across registries
- FDA 510(k) K991222 decided 9 Jul 1999 Active
- FDA GUDID UDI-DI 10381780520436 listed 1 Apr 2020 Listed
Timeline
- Cleared FDA 510(k) K991222
- Listed FDA GUDID 10381780520436
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Codman Microsensor®
- Generic name
- Ventricular cerebrospinal fluid drainage catheterization kit
- Model / Ref / Catalog
- 826633, 82-6633
- Primary DI / UDI-DI
- 10381780520436
- 510(k) Number
- FDA product code
- GWM
- GMDN term
- Ventricular cerebrospinal fluid drainage catheterization kit
- Device class
- Class II
- Regulation number
- 882.1620
- GUDID distribution status
- In Commercial Distribution
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