FDA Device Intelligence
Home › FHC, INC. › microTargeting™ Electrode and Insertion Tube Kit

microTargeting™ Electrode and Insertion Tube Kit

FHC, INC. · Model FC4001-00754 · UDI-DI 10873263007546

GZLHAW Prescription
2
510(k) clearances
227
Adverse events (3 deaths)
24
Recalls
24
Facilities

Description

microTargeting D.ZAP Electrode Kit, 5x, Sterile, Single, 1 Meg, for use with NexFrame and NexDrive or mT Drive. Each box contains: 2x MTDPLN(PA)(DB2) D.ZAP Differential Electrode. 1x IT(DB3) Insertion tube with Stylet. 1x PT(DB5) Protective Tube. Individual Specifications: MTDPLN(PA)(DB2) - 249.2mm electrode length, 10mm tip exposure, 234.2mm protective tube length, .56mm od, 1.0 meg DZAP(L) IT(DB3) - 194mm length, 1.8mm od, 1.6mm id, PT(DB5) - 194mm length, 1.47mm od, 0.99mm id

Recalls

DateFirmReason
2024-09-19Ad-Tech Medical Instrument CorporationAd-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style contact SD electrodes where the MR Conditional symbol was incorrectly p
2024-09-19Ad-Tech Medical Instrument CorporationAd-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style contact SD electrodes where the MR Conditional symbol was incorrectly p
2024-09-19Ad-Tech Medical Instrument CorporationAd-Tech is recalling these A-Style SD Depth Electrodes because a label discrepancy was identified on A style contact SD electrodes where the MR Conditional symbol was incorrectly p
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag
2021-12-09DIXI MEDICAL USAPotential deformation of the internal packaging (blister pack) could compromise sterile barrier of the device when removed from the Tyvek bag

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API keyRead the docs
Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.