Virginia National Guard 50DL-B
Virginia National Guard 50DL-B (Contec) is a Class II device made by Clinical Guard, cleared under FDA 510(k) K082641 on 10 Nov 2008 and listed in FDA GUDID since 15 Jan 2018 (UDI-DI 00851950008161), active as of 22 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 | Number00851950008161 | Date15 Jan 2018 | StatusListed |
| United States | FDA 510(k)SESE | NumberK082641 | Date10 Nov 2008 | StatusActive |
Official records
- AccessGUDID record 00851950008161
- FDA 510(k) database K082641
Across registries
- FDA 510(k) K082641 decided 10 Nov 2008 Active
- FDA GUDID UDI-DI 00851950008161 listed 15 Jan 2018 Listed
Timeline
- Cleared FDA 510(k) K082641
- Listed FDA GUDID 00851950008161
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Virginia National Guard
- Generic name
- Pulse oximeter
- Model / Ref / Catalog
- 50DL-B, Contec
- Description
- Contec CMS 50-DL Black Distributed by Clinical Guard
- Primary DI / UDI-DI
- 00851950008161
- 510(k) Number
- FDA product code
- DQA
- GMDN term
- Pulse oximeter
- Device class
- Class II
- Regulation number
- 870.2700
- GUDID distribution status
- In Commercial Distribution
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