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FDA 510(k)

Altapore MIS

K-Number: K201464 · 2020-06-30

ApplicantBaxter Healthcare Corporation
Decision Date2020-06-30
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Altapore MIS is the device name listed in this FDA 510(k) record. The listed applicant is Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2020-06-30 under 510(k) number K201464. 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 MIS?

Altapore MIS is a medical device that received FDA 510(k) clearance on 2020-06-30. The listed applicant is Baxter Healthcare Corporation. The 510(k) number is K201464.

When did Altapore MIS receive FDA 510(k) clearance?

Altapore MIS received FDA 510(k) clearance on 2020-06-30, under 510(k) number K201464.

Who is the listed applicant for Altapore MIS?

The FDA 510(k) record lists Baxter Healthcare Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Altapore MIS?

The FDA product code for Altapore MIS 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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