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FDA 510(k)

dpl SpotLite

K-Number: K183118 · 2019-02-07

ApplicantLed Technologies, Inc.
Decision Date2019-02-07
Product CodeOLP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

dpl SpotLite is the device name listed in this FDA 510(k) record. The listed applicant is Led Technologies, Inc.. It received FDA 510(k) clearance on 2019-02-07 under 510(k) number K183118. The device is classified under product code OLP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the dpl SpotLite?

dpl SpotLite is a medical device that received FDA 510(k) clearance on 2019-02-07. The listed applicant is Led Technologies, Inc.. The 510(k) number is K183118.

When did dpl SpotLite receive FDA 510(k) clearance?

dpl SpotLite received FDA 510(k) clearance on 2019-02-07, under 510(k) number K183118.

Who is the listed applicant for dpl SpotLite?

The FDA 510(k) record lists Led Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for dpl SpotLite?

The FDA product code for dpl SpotLite is OLP.

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Related Devices (Code: OLP)

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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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