FDA PMA

Device, hemostasis, vascular

PMA Number: P990037 · 2022-11-04

ApplicantVascular Solutions, Inc.

Decision Date2022-11-04

PMA NumberP990037

Product CodeMGB

Device ClassClass 3

Medical SpecialtyU

Advisory CommitteeCV

Device Summary

Device, hemostasis, vascular is the device name listed in this FDA 510(k) record. The listed applicant is Vascular Solutions, Inc.. It received FDA 510(k) clearance on 2022-11-04. The device is classified under product code MGB. It was reviewed by the CV advisory panel.

Frequently Asked Questions

What is the Device, hemostasis, vascular?

Device, hemostasis, vascular is a medical device that received FDA 510(k) clearance on 2022-11-04. The listed applicant is Vascular Solutions, Inc..

When did Device, hemostasis, vascular receive FDA 510(k) clearance?

The clearance date for Device, hemostasis, vascular can be found in the official FDA records.

Who is the listed applicant for Device, hemostasis, vascular?

The FDA 510(k) record lists Vascular Solutions, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Device, hemostasis, vascular?

The FDA product code for Device, hemostasis, vascular is MGB.

Related Clinical Trials

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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.