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FDA PMA

Lipoprotein, low density, removal

PMA Number: P940016 · 2019-06-07

ApplicantB. Braun Avitum AG
Decision Date2019-06-07
PMA NumberP940016
Product CodeMMY
Device ClassClass 3
Medical SpecialtyU
Advisory CommitteeGU

Device Summary

Lipoprotein, low density, removal is the device name listed in this FDA 510(k) record. The listed applicant is B. Braun Avitum AG. It received FDA 510(k) clearance on 2019-06-07. The device is classified under product code MMY. It was reviewed by the GU advisory panel.

Frequently Asked Questions

What is the Lipoprotein, low density, removal?

Lipoprotein, low density, removal is a medical device that received FDA 510(k) clearance on 2019-06-07. The listed applicant is B. Braun Avitum AG.

When did Lipoprotein, low density, removal receive FDA 510(k) clearance?

The clearance date for Lipoprotein, low density, removal can be found in the official FDA records.

Who is the listed applicant for Lipoprotein, low density, removal?

The FDA 510(k) record lists B. Braun Avitum AG as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Lipoprotein, low density, removal?

The FDA product code for Lipoprotein, low density, removal is MMY.

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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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