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FDA 510(k)

IMPROVED ENLIGHT LV

K-Number: K001881 · 2000-08-22

ApplicantSybron Dental Specialties, Inc.
Decision Date2000-08-22
Product CodeDYH
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPROVED ENLIGHT LV is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Dental Specialties, Inc.. It received FDA 510(k) clearance on 2000-08-22 under 510(k) number K001881. The device is classified under product code DYH. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPROVED ENLIGHT LV?

IMPROVED ENLIGHT LV is a medical device that received FDA 510(k) clearance on 2000-08-22. The listed applicant is Sybron Dental Specialties, Inc.. The 510(k) number is K001881.

When did IMPROVED ENLIGHT LV receive FDA 510(k) clearance?

IMPROVED ENLIGHT LV received FDA 510(k) clearance on 2000-08-22, under 510(k) number K001881.

Who is the listed applicant for IMPROVED ENLIGHT LV?

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

What is the FDA product code for IMPROVED ENLIGHT LV?

The FDA product code for IMPROVED ENLIGHT LV is DYH.

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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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