Inrad 620918
by Inrad
Inrad 620918 is a Class II device made by Inrad, cleared under FDA 510(k) K000612 on 24 Apr 2000 and listed in FDA GUDID since 8 Oct 2026 (UDI-DI 00817295021098), 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 | Number00817295021098 | Date8 Oct 2026 | StatusListed |
| United States | FDA 510(k)SESE | NumberK000612 | Date24 Apr 2000 | StatusActive |
Official records
- AccessGUDID record 00817295021098
- FDA 510(k) database K000612
Across registries
- FDA 510(k) K000612 decided 24 Apr 2000 Active
- FDA GUDID UDI-DI 00817295021098 listed 8 Oct 2026 Listed
Timeline
- Cleared FDA 510(k) K000612
- Listed FDA GUDID 00817295021098
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- Inrad
- Generic name
- End-cut biopsy gun handpiece/needle
- Model / Ref / Catalog
- 620918
- Primary DI / UDI-DI
- 00817295021098
- 510(k) Number
- FDA product code
- KNW, FCG
- GMDN term
- End-cut biopsy gun handpiece/needle
- Device class
- Class II
- Regulation number
- 876.1075
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
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