microTargeting™ Platform Accessory MP-KIT-A-PH

GUDID 00873263003794

Customized Phantom, for use with microTargeting Platform

FHC, INC.

Neurological stereotactic surgery system

• Primary Device ID: 00873263003794
• NIH Device Record Key: b8027978-9b63-4930-96f5-2a6805e7990d
• Commercial Distribution Discontinuation: 2019-06-24
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: microTargeting™ Platform Accessory
• Version Model Number: MP-KIT-A-PH-00379
• Catalog Number: MP-KIT-A-PH
• Company DUNS: 108179458
• Company Name: FHC, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: false
• Serial Number: true
• 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 Humidity: Between 10 Percent (%) Relative Humidity and 100 Percent (%) Relative Humidity
• Storage Environment Humidity: Between 10 Percent (%) Relative Humidity and 100 Percent (%) Relative Humidity

Device Identifiers

Device Issuing Agency	Device ID
GS1	00873263003794 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092192

FDA Product Code

• HAW: Neurological stereotaxic Instrument

Sterilization

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

[00873263003794]

Ethylene Oxide;Moist Heat or Steam Sterilization;Hydrogen Peroxide

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-06-24
• Device Publish Date: 2016-09-17

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