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FDA 510(k)

DMX

K-Number: K223550 · 2023-04-10

ApplicantDel Medical, Inc.
Decision Date2023-04-10
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DMX is a medical device manufactured by Del Medical, Inc.. It received FDA 510(k) clearance on 2023-04-10 under approval number K223550. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DMX?

DMX is a medical device that received FDA 510(k) clearance on 2023-04-10. It is manufactured by Del Medical, Inc.. The 510(k) number is K223550.

When was DMX approved by the FDA?

DMX received FDA 510(k) clearance on 2023-04-10, under approval number K223550.

What company makes DMX?

DMX is manufactured by Del Medical, Inc..

What is the FDA product code for DMX?

The FDA product code for DMX is KPR.

Other Devices by Del Medical, Inc.

K173018MDR17 Mobile Direct Radiographic System

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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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