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FDA 510(k)

ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT

K-Number: K925629 · 1993-11-23

ApplicantDen-Tal-Ez Mfg Co., Inc.
Decision Date1993-11-23
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Den-Tal-Ez Mfg Co., Inc.. It received FDA 510(k) clearance on 1993-11-23 under 510(k) number K925629. 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 ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT?

ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT is a medical device that received FDA 510(k) clearance on 1993-11-23. The listed applicant is Den-Tal-Ez Mfg Co., Inc.. The 510(k) number is K925629.

When did ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT receive FDA 510(k) clearance?

ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT received FDA 510(k) clearance on 1993-11-23, under 510(k) number K925629.

Who is the listed applicant for ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT?

The FDA 510(k) record lists Den-Tal-Ez Mfg Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT?

The FDA product code for ACCESSORY TO IMPROVED DENTAL OPERATING LIGHT is EAZ.

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Other records listing Den-Tal-Ez Mfg Co., Inc. as applicant

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.

K932824EVACUATOR, ORAL CAVITYK931204AS3000 OPERATIVE DENTAL UNIT (DELIVERY SYSTEM)K920016IMPROVED DENTAL CHAIRK920017IMPROVED DENTAL OPERATING LIGHTK874294AUTOCHUCK ATTACHMENTK780469PANORAMIC X-RAY, DENTAL

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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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