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FDA 510(k)

ALTAPORE SHAPE

K-Number: K200640 · 2020-05-08

ApplicantBaxter Healthcare Corporation
Decision Date2020-05-08
Product CodeMQV
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALTAPORE SHAPE is a medical device manufactured by Baxter Healthcare Corporation. It received FDA 510(k) clearance on 2020-05-08 under approval number K200640. 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 SHAPE?

ALTAPORE SHAPE is a medical device that received FDA 510(k) clearance on 2020-05-08. It is manufactured by Baxter Healthcare Corporation. The 510(k) number is K200640.

When was ALTAPORE SHAPE approved by the FDA?

ALTAPORE SHAPE received FDA 510(k) clearance on 2020-05-08, under approval number K200640.

What company makes ALTAPORE SHAPE?

ALTAPORE SHAPE is manufactured by Baxter Healthcare Corporation.

What is the FDA product code for ALTAPORE SHAPE?

The FDA product code for ALTAPORE SHAPE 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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