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FDA 510(k)

V-STICK VASCULAR ACCESS SET

K-Number: K130730 · 2013-11-22

ApplicantArgon Medical
Decision Date2013-11-22
Product CodeDYB
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

V-STICK VASCULAR ACCESS SET is the device name listed in this FDA 510(k) record. The listed applicant is Argon Medical. It received FDA 510(k) clearance on 2013-11-22 under 510(k) number K130730. 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 V-STICK VASCULAR ACCESS SET?

V-STICK VASCULAR ACCESS SET is a medical device that received FDA 510(k) clearance on 2013-11-22. The listed applicant is Argon Medical. The 510(k) number is K130730.

When did V-STICK VASCULAR ACCESS SET receive FDA 510(k) clearance?

V-STICK VASCULAR ACCESS SET received FDA 510(k) clearance on 2013-11-22, under 510(k) number K130730.

Who is the listed applicant for V-STICK VASCULAR ACCESS SET?

The FDA 510(k) record lists Argon Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V-STICK VASCULAR ACCESS SET?

The FDA product code for V-STICK VASCULAR ACCESS SET is DYB.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Related Devices (Code: DYB)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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