Altapore
K-Number: K192363 · 2020-01-09
ApplicantBaxter Healthcare Corporation
Decision Date2020-01-09
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Altapore is a medical device manufactured by Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2020-01-09 under approval number K192363. The device is classified under product code MQV. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Altapore?
Altapore is a medical device that received FDA 510(k) clearance on 2020-01-09. It is manufactured by Baxter Healthcare Corporation. The 510(k) number is K192363.
When was Altapore approved by the FDA?
Altapore received FDA 510(k) clearance on 2020-01-09, under approval number K192363.
What company makes Altapore?
Altapore is manufactured by Baxter Healthcare Corporation.
What is the FDA product code for Altapore?
The FDA product code for Altapore is MQV.
Other Devices by Baxter Healthcare Corporation
Related Devices (Code: MQV)
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.