Preview Treatment Planning Software

GUDID B119PREVIEW0

M2S, INC.

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• Primary Device ID: B119PREVIEW0
• NIH Device Record Key: 2fa059d6-02d5-4e70-9cd7-ccb7ed00e7fa
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Preview Treatment Planning Software
• Version Model Number: 4.x
• Company DUNS: 794577288
• Company Name: M2S, 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: 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: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com
• Phone: 603-298-5509
• Email: customerservice@m2s.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B119PREVIEW0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K040852

FDA Product Code

• LLZ: System, Image Processing, Radiological

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-01-16
• Device Publish Date: 2016-09-23