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FDA 510(k)

RMO PLASMA CURING LIGHT

K-Number: K024374 · 2003-03-10

ApplicantLokki Lasers Medicaux
Decision Date2003-03-10
Product CodeEBZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RMO PLASMA CURING LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Lokki Lasers Medicaux. It received FDA 510(k) clearance on 2003-03-10 under 510(k) number K024374. The device is classified under product code EBZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RMO PLASMA CURING LIGHT?

RMO PLASMA CURING LIGHT is a medical device that received FDA 510(k) clearance on 2003-03-10. The listed applicant is Lokki Lasers Medicaux. The 510(k) number is K024374.

When did RMO PLASMA CURING LIGHT receive FDA 510(k) clearance?

RMO PLASMA CURING LIGHT received FDA 510(k) clearance on 2003-03-10, under 510(k) number K024374.

Who is the listed applicant for RMO PLASMA CURING LIGHT?

The FDA 510(k) record lists Lokki Lasers Medicaux as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RMO PLASMA CURING LIGHT?

The FDA product code for RMO PLASMA CURING LIGHT is EBZ.

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Related Devices (Code: EBZ)

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

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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