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FDA 510(k)

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set

K-Number: K202141 · 2021-01-15

ApplicantArgon Medical Devices, Inc.
Decision Date2021-01-15
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is a medical device manufactured by Argon Medical Devices, Inc.. It received FDA 510(k) clearance on 2021-01-15 under approval number K202141. The device is classified under product code DYB. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is a medical device that received FDA 510(k) clearance on 2021-01-15. It is manufactured by Argon Medical Devices, Inc.. The 510(k) number is K202141.

When was Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set approved by the FDA?

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set received FDA 510(k) clearance on 2021-01-15, under approval number K202141.

What company makes Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is manufactured by Argon Medical Devices, Inc..

What is the FDA product code for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set?

The FDA product code for Scorpion Stylet Portal Vein Access Set, Scorpion Needle Portal Vein Access Set is DYB.

Related Clinical Trials

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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