s5i Control Console

GUDID 00184360000709

VOLCANO CORPORATION

Cardiovascular ultrasound imaging system

• Primary Device ID: 00184360000709
• NIH Device Record Key: 46ceb344-47ac-456f-a3c6-6644d29caf7e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: s5i Control Console
• Version Model Number: 806302012
• Company DUNS: 135179237
• Company Name: VOLCANO CORPORATION
• 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
GS1	00184360000709 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K071554

FDA Product Code

• OBJ: Catheter, Ultrasound, Intravascular

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: 2016-09-19

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