Quiver Aspiration Pump
K-Number: K232831 · 2024-02-22
Device Summary
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. The listed applicant is Anoxia Medical, Inc.. The 510(k) number is K232831.
When did Quiver Aspiration Pump receive FDA 510(k) clearance?
Quiver Aspiration Pump received FDA 510(k) clearance on 2024-02-22, under 510(k) number K232831.
Who is the listed applicant for Quiver Aspiration Pump?
The FDA 510(k) record lists Anoxia Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Quiver Aspiration Pump?
The FDA product code for Quiver Aspiration Pump is BTA.
Other records listing Anoxia Medical, Inc. as applicant
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: BTA)
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.