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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 the device name listed in this FDA 510(k) record. The listed applicant is Luvo Medical Technologies, Inc.. It received FDA 510(k) clearance on 2020-03-05 under 510(k) 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. The listed applicant is Luvo Medical Technologies, Inc.. The 510(k) number is K193072.

When did Lucent : IPL receive FDA 510(k) clearance?

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

Who is the listed applicant for Lucent : IPL?

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

What is the FDA product code for Lucent : IPL?

The FDA product code for Lucent : IPL is ONF.

Other records listing Luvo Medical Technologies, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Related Devices (Code: ONF)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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