Unolok 23 G X ¾"
by Hindustan Syringes and Medical Devices Limited
Unolok 23 G X ¾" (00328) is a Class II device made by Hindustan Syringes and Medical Devices Limited, cleared under FDA 510(k) K953252 on 26 Nov 1996 and listed in FDA GUDID since 9 Jan 2017 (UDI-DI 08903347003289), 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 | Number08903347003289 | Date9 Jan 2017 | StatusListed |
| United States | FDA 510(k)SESE | NumberK953252 | Date26 Nov 1996 | StatusActive |
Official records
- AccessGUDID record 08903347003289
- FDA 510(k) database K953252
Across registries
- FDA 510(k) K953252 decided 26 Nov 1996 Active
- FDA GUDID UDI-DI 08903347003289 listed 9 Jan 2017 Listed
Timeline
- Cleared FDA 510(k) K953252
- Listed FDA GUDID 08903347003289
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Unolok
- Generic name
- Venous butterfly needle/set
- Model / Ref / Catalog
- 23 G X ¾", 00328
- Description
- UNOLOK Luer Lock Infusion Sets,23 G X ¾" (0.60 X19MM ) 12" TUBE MYCO RE-ORDER # 7001-23
- Primary DI / UDI-DI
- 08903347003289
- 510(k) Number
- FDA product code
- FOZ
- GMDN term
- Venous butterfly needle/set
- Device class
- Class II
- Regulation number
- 880.5200
- GUDID distribution status
- In Commercial Distribution
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