Lifeguard Vision

GUDID H787LGV2075Y5

LIFEGUARD VISION Safety Needle

ANGIODYNAMICS, INC.

Vascular port administration set

• Primary Device ID: H787LGV2075Y5
• NIH Device Record Key: b89f0843-8e9a-47e0-9942-2505f8adc1ca
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lifeguard Vision
• Version Model Number: LGV-20-75Y
• Company DUNS: 601994184
• Company Name: ANGIODYNAMICS, INC.
• Device Count: 20
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com

Device Dimensions

• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch
• Needle Gauge: 22 Gauge
• Length: 0.8 Inch

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	H787LGV2075Y0 [Unit of Use]
HIBCC	H787LGV2075Y5 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K013871

FDA Product Code

• FPA: Set, administration, intravascular

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-09-20

On-Brand Devices [Lifeguard Vision]

• H787LGV22755: LIFEGUARD VISION Safety Needle
• H787LGV2075Y5: LIFEGUARD VISION Safety Needle