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FDA 510(k)

Quiver Aspiration Pump

K-Number: K232831 · 2024-02-22

ApplicantAnoxia Medical, Inc.
Decision Date2024-02-22
Product CodeBTA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Quiver Aspiration Pump is a medical device manufactured by Anoxia Medical, Inc.. It received FDA 510(k) clearance on 2024-02-22 under approval number K232831. The device is classified under product code BTA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Quiver Aspiration Pump?

Quiver Aspiration Pump is a medical device that received FDA 510(k) clearance on 2024-02-22. It is manufactured by Anoxia Medical, Inc.. The 510(k) number is K232831.

When was Quiver Aspiration Pump approved by the FDA?

Quiver Aspiration Pump received FDA 510(k) clearance on 2024-02-22, under approval number K232831.

What company makes Quiver Aspiration Pump?

Quiver Aspiration Pump is manufactured by Anoxia Medical, Inc..

What is the FDA product code for Quiver Aspiration Pump?

The FDA product code for Quiver Aspiration Pump is BTA.

Other Devices by Anoxia Medical, Inc.

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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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