Inrad 41820
by Inrad
Inrad 41820 is a Class I device made by Inrad, cleared under FDA 510(k) K813368 on 5 Jan 1982 and listed in FDA GUDID since 9 Oct 2026 (UDI-DI 00817295020220), active as of 23 Oct 2026. One FDA recall is linked to it.
Active
510(k)
Valid until
No expiry
FDA recalls
None ongoingDocuments
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00817295020220 | Date9 Oct 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK813368 | Date5 Jan 1982 | StatusActive |
Official records
- AccessGUDID record 00817295020220
- FDA 510(k) database K813368
Across registries
- FDA 510(k) K813368 decided 5 Jan 1982 Active
- FDA GUDID UDI-DI 00817295020220 listed 9 Oct 2026 Listed
Recalls
-
- Terminated Z-1063-2011
This lot of product has the wrong expiration date on the carton label. The pouches contained the correct expiration date.
Timeline
- Cleared FDA 510(k) K813368
- Recall initiated FDA recalls Z-1063-2011
- Listed FDA GUDID 00817295020220
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- Withdrawn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
- 41820
- Primary DI / UDI-DI
- 00817295020220
- 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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