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FDA 510(k)

DENTAL LIGHT

K-Number: K772351 · 1978-01-17

ApplicantChemetron Dental Products
Decision Date1978-01-17
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Chemetron Dental Products. It received FDA 510(k) clearance on 1978-01-17 under 510(k) number K772351. 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 DENTAL LIGHT?

DENTAL LIGHT is a medical device that received FDA 510(k) clearance on 1978-01-17. The listed applicant is Chemetron Dental Products. The 510(k) number is K772351.

When did DENTAL LIGHT receive FDA 510(k) clearance?

DENTAL LIGHT received FDA 510(k) clearance on 1978-01-17, under 510(k) number K772351.

Who is the listed applicant for DENTAL LIGHT?

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

What is the FDA product code for DENTAL LIGHT?

The FDA product code for DENTAL LIGHT is EAZ.

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Related Devices (Code: EAZ)

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.

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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