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FDA 510(k)

dpl Faceware

K-Number: K183247 · 2019-03-14

ApplicantLed Technologies, Inc.
Decision Date2019-03-14
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

dpl Faceware is a medical device manufactured by Led Technologies, Inc.. It received FDA 510(k) clearance on 2019-03-14 under approval number K183247. The device is classified under product code OHS. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the dpl Faceware?

dpl Faceware is a medical device that received FDA 510(k) clearance on 2019-03-14. It is manufactured by Led Technologies, Inc.. The 510(k) number is K183247.

When was dpl Faceware approved by the FDA?

dpl Faceware received FDA 510(k) clearance on 2019-03-14, under approval number K183247.

What company makes dpl Faceware?

dpl Faceware is manufactured by Led Technologies, Inc..

What is the FDA product code for dpl Faceware?

The FDA product code for dpl Faceware is OHS.

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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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