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FDA 510(k)

SelectFlex Neurovascular Access System Family

K-Number: K230322 · 2023-06-22

Decision Date2023-06-22
Product CodeQJP
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SelectFlex Neurovascular Access System Family is a medical device manufactured by Q'Apel Medical, Inc.. It received FDA 510(k) clearance on 2023-06-22 under approval number K230322. The device is classified under product code QJP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SelectFlex Neurovascular Access System Family?

SelectFlex Neurovascular Access System Family is a medical device that received FDA 510(k) clearance on 2023-06-22. It is manufactured by Q'Apel Medical, Inc.. The 510(k) number is K230322.

When was SelectFlex Neurovascular Access System Family approved by the FDA?

SelectFlex Neurovascular Access System Family received FDA 510(k) clearance on 2023-06-22, under approval number K230322.

What company makes SelectFlex Neurovascular Access System Family?

SelectFlex Neurovascular Access System Family is manufactured by Q'Apel Medical, Inc..

What is the FDA product code for SelectFlex Neurovascular Access System Family?

The FDA product code for SelectFlex Neurovascular Access System Family is QJP.

Related Clinical Trials

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Official Source

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