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FDA 510(k)

LUNA-VUE DENTAL OPERATING LIGHT

K-Number: K801683 · 1980-08-04

ApplicantPacific Dental Corp.
Decision Date1980-08-04
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LUNA-VUE DENTAL OPERATING LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Pacific Dental Corp.. It received FDA 510(k) clearance on 1980-08-04 under 510(k) number K801683. The device is classified under product code EAZ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LUNA-VUE DENTAL OPERATING LIGHT?

LUNA-VUE DENTAL OPERATING LIGHT is a medical device that received FDA 510(k) clearance on 1980-08-04. The listed applicant is Pacific Dental Corp.. The 510(k) number is K801683.

When did LUNA-VUE DENTAL OPERATING LIGHT receive FDA 510(k) clearance?

LUNA-VUE DENTAL OPERATING LIGHT received FDA 510(k) clearance on 1980-08-04, under 510(k) number K801683.

Who is the listed applicant for LUNA-VUE DENTAL OPERATING LIGHT?

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

What is the FDA product code for LUNA-VUE DENTAL OPERATING LIGHT?

The FDA product code for LUNA-VUE DENTAL OPERATING LIGHT is EAZ.

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Related Devices (Code: EAZ)

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K072309MICROLUX/BLUAddent, Inc.K041614MICROLUX DLAddent, Inc.K033033VIZILITE-BLUE ORAL EXAM KITTrylon Corp.K003995SPECULITE/ORALLITETrylon Corp.K926081DENTAL LIGHTMdt Corp., Inc.K935390SIROLUX FANTASTICPelton & Crane Co.

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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