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FDA 510(k)

MGP 15 DICOM THEATER

K-Number: K042942 · 2004-11-22

ApplicantBarco NV Barcoview
Decision Date2004-11-22
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MGP 15 DICOM THEATER is the device name listed in this FDA 510(k) record. The listed applicant is Barco NV Barcoview. It received FDA 510(k) clearance on 2004-11-22 under 510(k) number K042942. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MGP 15 DICOM THEATER?

MGP 15 DICOM THEATER is a medical device that received FDA 510(k) clearance on 2004-11-22. The listed applicant is Barco NV Barcoview. The 510(k) number is K042942.

When did MGP 15 DICOM THEATER receive FDA 510(k) clearance?

MGP 15 DICOM THEATER received FDA 510(k) clearance on 2004-11-22, under 510(k) number K042942.

Who is the listed applicant for MGP 15 DICOM THEATER?

The FDA 510(k) record lists Barco NV Barcoview as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MGP 15 DICOM THEATER?

The FDA product code for MGP 15 DICOM THEATER is LLZ.

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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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