Identity
- Trade Name
- microTargeting™ Electrode Cable FDA UDI
- Generic Name
- Depth electrode FDA UDI
- Device Name
- microTargeting Electrode Cable w/ Alligator Clips, Sterile, for use with microTargeting Electrodes FDA UDI
- Model / Reference
- 66-EL-EC-01-00257 FDA UDI
- Description
- microTargeting Electrode Cable w/ Alligator Clips, Sterile, for use with microTargeting Electrodes FDA UDI
Identifiers
- Catalog Number
- 66-EL-EC-01 FDA UDI
- Primary DI / UDI-DI
- 00873263002575 FDA UDI
- 510(k) Number
- K071364 FDA UDI
- FDA Product Code
- GZL FDA UDI
- GMDN Term
- Depth electrode FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 882.1330 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
Yes
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
No
FDA UDI
Lot / Batch Number
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Ethylene Oxide FDA UDI
MR Unsafe FDA UDI
Category: Depth electrode
microTargeting™ Electrode Cable by Fhc, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K071364 also covers:
- Guideline™ 4000 — FHC, INC.
- Lead Adapter, For use with Multi-Lead Trial Cable to Guideline System — FHC, INC.
- microTargeting ™ Lead Adapter — FHC, INC.
- microTargeting™ Electrode Cable — FHC, INC.
- microTargeting™ Electrode Cable — FHC, INC.
- microTargeting™ Electrode Cable — FHC, INC.
- microTargeting™ Electrode Cable — FHC, INC.
- microTargeting™ Guideline 4000 LP+™ — FHC, INC.
- microTargeting™ Guideline 4000 LP+™ Breakout Box — FHC, INC.
- microTargeting™ Guideline 4000 LP+™ Cart — FHC, INC.
- microTargeting™ Guideline 4000 LP+™ Channel Card — FHC, INC.
- microTargeting™ LP+ Electrode Cable — FHC, INC.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Fhc, Inc.
Sources (1)
- FDA UDI e346c7ae-01e6-44f9-977e-8709f7e357a1 37 fields · synced May 30, 2026