microTargeting™ Array Electrode 22375Z-00790
by Fhc, Inc.
microTargeting™ Array Electrode 22375Z-00790 is a Class II device made by Fhc, Inc., cleared under FDA 510(k) K033173 on 24 Mar 2004 and listed in FDA GUDID since 24 Aug 2019 (UDI-DI 00873263007907), 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 | Number00873263007907 | Date24 Aug 2019 | StatusListed |
| United States | FDA 510(k)SESE | NumberK033173 | Date24 Mar 2004 | StatusActive |
Official records
- AccessGUDID record 00873263007907
- FDA 510(k) database K033173
Across registries
- FDA 510(k) K033173 decided 24 Mar 2004 Active
- FDA GUDID UDI-DI 00873263007907 listed 24 Aug 2019 Listed
Timeline
- Cleared FDA 510(k) K033173
- Listed FDA GUDID 00873263007907
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- Trade name
- microTargeting™ Array Electrode
- Generic name
- Depth electrode
- Model / Ref / Catalog
- 22375Z-00790, 22375Z
- Primary DI / UDI-DI
- 00873263007907
- 510(k) Number
- FDA product code
- GZL
- GMDN term
- Depth electrode
- Device class
- Class II
- Regulation number
- 882.1330
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Ethylene Oxide
- MRI safety
- MR Unsafe
- Size
- Length — 268.5 MillimeterOuter Diameter — 0.55 MillimeterLength — 3 MillimeterLength — 276.5 Millimeter