Network NS40300
by Network Medical Products, Ltd.
Network NS40300 is a Class II device made by Network Medical Products, Ltd., cleared under FDA 510(k) K130117 on 29 Oct 2013 and listed in FDA GUDID since 25 Feb 2020 (UDI-DI 05056100706996), 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 | Number05056100706996 | Date25 Feb 2020 | StatusListed |
| United States | FDA 510(k)SESE | NumberK130117 | Date29 Oct 2013 | StatusActive |
Official records
- AccessGUDID record 05056100706996
- FDA 510(k) database K130117
Across registries
- FDA 510(k) K130117 decided 29 Oct 2013 Active
- FDA GUDID UDI-DI 05056100706996 listed 25 Feb 2020 Listed
Timeline
- Cleared FDA 510(k) K130117
- Listed FDA GUDID 05056100706996
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Network
- Generic name
- Ophthalmic sponge
- Model / reference
- NS40300
- Primary DI / UDI-DI
- 05056100706996
- 510(k) Number
- FDA product code
- HOZ
- GMDN term
- Ophthalmic sponge
- Device class
- Class II
- Regulation number
- 886.4790
- GUDID distribution status
- In Commercial Distribution
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