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FDA 510(k)

Lucent : IPL

K-Number: K193072 · 2020-03-05

ApplicantLuvo Medical Technologies, Inc.
Decision Date2020-03-05
Product CodeONF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Lucent : IPL is a medical device manufactured by Luvo Medical Technologies, Inc.. It received FDA 510(k) clearance on 2020-03-05 under approval number K193072. The device is classified under product code ONF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Lucent : IPL?

Lucent : IPL is a medical device that received FDA 510(k) clearance on 2020-03-05. It is manufactured by Luvo Medical Technologies, Inc.. The 510(k) number is K193072.

When was Lucent : IPL approved by the FDA?

Lucent : IPL received FDA 510(k) clearance on 2020-03-05, under approval number K193072.

What company makes Lucent : IPL?

Lucent : IPL is manufactured by Luvo Medical Technologies, Inc..

What is the FDA product code for Lucent : IPL?

The FDA product code for Lucent : IPL is ONF.

Other Devices by Luvo Medical Technologies, Inc.

K193446Bare: 808 K212607Darwin K210129RF Thermal System K203728Darwin

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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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