FDA 510(k)

RYTHMIC AND RYTHMIC UV

K-Number: K003170 · 2000-12-15

Decision Date2000-12-15

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

RYTHMIC AND RYTHMIC UV is the device name listed in this FDA 510(k) record. The listed applicant is Essilor Intl.. It received FDA 510(k) clearance on 2000-12-15 under 510(k) number K003170. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RYTHMIC AND RYTHMIC UV?

RYTHMIC AND RYTHMIC UV is a medical device that received FDA 510(k) clearance on 2000-12-15. The listed applicant is Essilor Intl.. The 510(k) number is K003170.

When did RYTHMIC AND RYTHMIC UV receive FDA 510(k) clearance?

RYTHMIC AND RYTHMIC UV received FDA 510(k) clearance on 2000-12-15, under 510(k) number K003170.

Who is the listed applicant for RYTHMIC AND RYTHMIC UV?

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

What is the FDA product code for RYTHMIC AND RYTHMIC UV?

The FDA product code for RYTHMIC AND RYTHMIC UV is LPL.

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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.