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FDA 510(k)

dpl II Panel

K-Number: K171390 · 2017-08-03

ApplicantLed Technologies, Inc.
Decision Date2017-08-03
Product CodeOHS
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

dpl II Panel is a medical device manufactured by Led Technologies, Inc.. It received FDA 510(k) clearance on 2017-08-03 under approval number K171390. 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 II Panel?

dpl II Panel is a medical device that received FDA 510(k) clearance on 2017-08-03. It is manufactured by Led Technologies, Inc.. The 510(k) number is K171390.

When was dpl II Panel approved by the FDA?

dpl II Panel received FDA 510(k) clearance on 2017-08-03, under approval number K171390.

What company makes dpl II Panel?

dpl II Panel is manufactured by Led Technologies, Inc..

What is the FDA product code for dpl II Panel?

The FDA product code for dpl II Panel is OHS.

Other Devices by Led Technologies, Inc.

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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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