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FDA 510(k)

ALTAPORE

K-Number: K181225 · 2018-08-31

ApplicantBaxter Healthcare Corporation
Decision Date2018-08-31
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 2018-08-31 under approval number K181225. 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 2018-08-31. It is manufactured by Baxter Healthcare Corporation. The 510(k) number is K181225.

When was ALTAPORE approved by the FDA?

ALTAPORE received FDA 510(k) clearance on 2018-08-31, under approval number K181225.

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.

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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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