microTargeting™ Array Electrode Carrier and Clamp FC1021

GUDID 00873263000618

Array Electrode Carrier and Clamp for microTargeting(TM) Drive

FHC, INC.

Neurosurgical micro targeting drive

• Primary Device ID: 00873263000618
• NIH Device Record Key: 96251f76-9f26-4b0b-93ad-e03d3825c606
• Commercial Distribution Discontinuation: 2018-07-13
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: microTargeting™ Array Electrode Carrier and Clamp
• Version Model Number: FC1021-00061
• Catalog Number: FC1021
• Company DUNS: 108179458
• Company Name: FHC, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com

Operating and Storage Conditions

• Storage Environment Temperature: Between -34 Degrees Celsius and 57 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00873263000618 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K011775

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

• Steralize Prior To Use: true
• Device Is Sterile: false

[00873263000618]

Moist Heat or Steam Sterilization;Hydrogen Peroxide;Ethylene Oxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-16
• Device Publish Date: 2016-08-22

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• 00873263008904 - microTargeting™ Single Procedure Kit: 2025-05-08 microTargeting Single Procedure Kit, with microElectrode, tubes, sterile drape sleeve and cable. Contains: IT(BP2): Insertion Tu
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