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FDA 510(k)

MMPC-4127F1

K-Number: K172922 · 2017-12-21

ApplicantBarco N.V.
Decision Date2017-12-21
Product CodePZZ
Advisory CommitteePA
DecisionSubstantially Equivalent

Device Summary

MMPC-4127F1 is a medical device manufactured by Barco N.V.. It received FDA 510(k) clearance on 2017-12-21 under approval number K172922. The device is classified under product code PZZ. It was reviewed by the PA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MMPC-4127F1?

MMPC-4127F1 is a medical device that received FDA 510(k) clearance on 2017-12-21. It is manufactured by Barco N.V.. The 510(k) number is K172922.

When was MMPC-4127F1 approved by the FDA?

MMPC-4127F1 received FDA 510(k) clearance on 2017-12-21, under approval number K172922.

What company makes MMPC-4127F1?

MMPC-4127F1 is manufactured by Barco N.V..

What is the FDA product code for MMPC-4127F1?

The FDA product code for MMPC-4127F1 is PZZ.

Other Devices by Barco N.V.

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Related Devices (Code: PZZ)

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.