Anivia SG1000 Pump Console
K-Number: K230698 · 2023-04-18
ApplicantApmtd, Inc.
Decision Date2023-04-18
Product CodeDWA
Advisory CommitteeCV
DecisionSubstantially Equivalent
Device Summary
Anivia SG1000 Pump Console is a medical device manufactured by Apmtd, Inc.. It received FDA 510(k) clearance on 2023-04-18 under approval number K230698. The device is classified under product code DWA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Anivia SG1000 Pump Console?
Anivia SG1000 Pump Console is a medical device that received FDA 510(k) clearance on 2023-04-18. It is manufactured by Apmtd, Inc.. The 510(k) number is K230698.
When was Anivia SG1000 Pump Console approved by the FDA?
Anivia SG1000 Pump Console received FDA 510(k) clearance on 2023-04-18, under approval number K230698.
What company makes Anivia SG1000 Pump Console?
Anivia SG1000 Pump Console is manufactured by Apmtd, Inc..
What is the FDA product code for Anivia SG1000 Pump Console?
The FDA product code for Anivia SG1000 Pump Console is DWA.
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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.