Inrad 15425
by Inrad
Inrad 15425 is a Class I device made by Inrad, cleared under FDA 510(k) K896019 on 3 Jan 1990 and listed in FDA GUDID since 8 Oct 2026 (UDI-DI 00817295020015), 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 | Number00817295020015 | Date8 Oct 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK896019 | Date3 Jan 1990 | StatusActive |
Official records
- AccessGUDID record 00817295020015
- FDA 510(k) database K896019
Across registries
- FDA 510(k) K896019 decided 3 Jan 1990 Active
- FDA GUDID UDI-DI 00817295020015 listed 8 Oct 2026 Listed
Timeline
- Cleared FDA 510(k) K896019
- Listed FDA GUDID 00817295020015
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Inrad
- Generic name
- Body aspiration needle, single-use
- Model / Ref / Catalog
- 15425
- Primary DI / UDI-DI
- 00817295020015
- 510(k) Number
- FDA product code
- GAA
- GMDN term
- Body aspiration needle, single-use
- Device class
- Class I
- Regulation number
- 878.4800
- GUDID distribution status
- In Commercial Distribution
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