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microTargeting™ Electrode 35325Z-00949

by Fhc, Inc. GUDID

Listed FDA GUDID listing, no authorization on record

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10873263009496 UDI-DIDate2 Dec 2025ListedStatusListed GUDID: in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Recalls

0 recalls · FDA

No FDA recalls on record, checked 23 Oct 2026.

Specification

GUDID

Trade Name
microTargeting™ Electrode
Generic Name
Depth electrode
Model / Ref / Catalog
35325Z-00949, 35325Z
Primary DI / UDI-DI
10873263009496
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
Sterilization Method
Moist Heat or Steam Sterilization
MRI Safety
MR Conditional
Size
Outer Diameter — 0.86 Millimeter
Length — 271.4 Millimeter
Length — 263.4 Millimeter
Length — 3 Millimeter

Related devices

Cleared under the same submission (K033173)

Show all (12)

Other devices from Fhc, Inc.

See all devices from Fhc, Inc. →

Properties

  • Single Use
  • Prescription Use
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No