FLUOBEAM 800

GUDID B475FB800CLV180

FLUOPTICS

Stationary general-purpose fluoroscopic x-ray system, digital

• Primary Device ID: B475FB800CLV180
• NIH Device Record Key: 0fe2980a-b011-4e05-a213-3d0da8c26da3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FLUOBEAM 800
• Version Model Number: FB800-CL v1.8
• Company DUNS: 260631677
• Company Name: FLUOPTICS
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B475FB800CLV180 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132475

FDA Product Code

• OWN: Confocal Optical Imaging

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-04-27

On-Brand Devices [FLUOBEAM 800]

• B475FB800CLV190: FB800-CL v1.9
• B475FB800CLV180: FB800-CL v1.8