Stopcock 196590

GUDID 20886333208665

3 Way Stopcock w/ Rotating Adapter(1050psi)

ARGON MEDICAL DEVICES, INC.

Intravenous line stopcock Intravenous line stopcock

• Primary Device ID: 20886333208665
• NIH Device Record Key: f38ebccb-66e8-4b0f-b289-965b49f5850b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Stopcock
• Version Model Number: 196590
• Catalog Number: 196590
• Company DUNS: 140727624
• Company Name: ARGON MEDICAL DEVICES, 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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: 1.800.927.4669
• Email: Customer.Service@argonmedical.com
• Phone: 1.800.927.4669
• Email: Customer.Service@argonmedical.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886333208661 [Primary]
GS1	20886333208665 [Package]; Contains: 00886333208661; Package: Box [25 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K915301

FDA Product Code

• DTL: Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-20

On-Brand Devices [Stopcock]

• 20886333208665: 3 Way Stopcock w/ Rotating Adapter(1050psi)
• 20886333201413: Clear, 1-Way Stopcock w/ Male Luer Lock