Resident Expert Software Module C0258

GUDID 00873263008188

Guideline 4000™ Resident Expert Software Module, 1x

FHC, INC.

Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system Neurophysiologic monitoring system

• Primary Device ID: 00873263008188
• NIH Device Record Key: bd555fad-2e3d-4208-af8c-998e9bb3585a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Resident Expert Software Module
• Version Model Number: C0258-00818
• Catalog Number: C0258
• 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• 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
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com
• Phone: +1(800)326-2905
• Email: fhcinc@fh-co.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00873263008188 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K183123

FDA Product Code

• GZL: ELECTRODE, DEPTH

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-08-18
• Device Publish Date: 2020-08-10

On-Brand Devices [Resident Expert Software Module]

• 00873263008089: Guideline 4000™ Resident Expert Software Module, 1x
• 00873263008188: Guideline 4000™ Resident Expert Software Module, 1x