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FDA 510(k)

Altapore

K-Number: K192363 · 2020-01-09

ApplicantBaxter Healthcare Corporation
Decision Date2020-01-09
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Altapore 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 2020-01-09 under 510(k) 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. The listed applicant is Baxter Healthcare Corporation. The 510(k) number is K192363.

When did Altapore receive FDA 510(k) clearance?

Altapore received FDA 510(k) clearance on 2020-01-09, under 510(k) number K192363.

Who is the listed applicant for Altapore?

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?

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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