Medline MDS611930AG
Medline MDS611930AG is a Class II device made by Medline Industries, Inc., cleared under FDA 510(k) K020003 on 7 Nov 2002 and listed in FDA GUDID since 8 Dec 2020 (UDI-DI 10888277657694), 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 | Number10888277657694 | Date8 Dec 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK020003 | Date7 Nov 2002 | StatusActive |
Official records
- AccessGUDID record 10888277657694
- FDA 510(k) database K020003
Across registries
- FDA 510(k) K020003 decided 7 Nov 2002 Active
- FDA GUDID UDI-DI 10888277657694 listed 8 Dec 2020 Listed
Timeline
- Cleared FDA 510(k) K020003
- Listed FDA GUDID 10888277657694
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Medline
- Generic name
- Electrocardiographic electrode, single-use
- Model / Ref / Catalog
- MDS611930AG
- Primary DI / UDI-DI
- 10888277657694
- 510(k) Number
- FDA product code
- DRX
- GMDN term
- Electrocardiographic electrode, single-use
- Device class
- Class II
- Regulation number
- 870.2360
- GUDID distribution status
- In Commercial Distribution
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