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FDA 510(k)

A-DEC DENTAL LIGHT

K-Number: K893044 · 1989-07-14

ApplicantA-Dec, Inc.
Decision Date1989-07-14
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

A-DEC DENTAL LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is A-Dec, Inc.. It received FDA 510(k) clearance on 1989-07-14 under 510(k) number K893044. 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 A-DEC DENTAL LIGHT?

A-DEC DENTAL LIGHT is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is A-Dec, Inc.. The 510(k) number is K893044.

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

A-DEC DENTAL LIGHT received FDA 510(k) clearance on 1989-07-14, under 510(k) number K893044.

Who is the listed applicant for A-DEC DENTAL LIGHT?

The FDA 510(k) record lists A-Dec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for A-DEC DENTAL LIGHT?

The FDA product code for A-DEC DENTAL LIGHT is EAZ.

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Other records listing A-Dec, 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.

K213932A-dec 300, A-dec 500K102234A-DEC 200 DENTAL SYSTEMK100647A-DEC/W&H SYNEA SONIC SCALER HANDPIECE, MODELS ZA-55, ZA-55 L, ZA-55 LM, ZA-55M, SF1LMK082716A-DEC/W&H ALEGRA AIR-DRIVEN HIGHSPEED HANDPIECE, MODEL TE-97, TE-98, A-DEC/W&H ALEGRA HANDPIECE ATTACHMENT, MODEL HE-43K082827A-DEC/W&H PROFIN RECIPROCATING CONTRA-ANGLE HANDPIECE ATTACHMENTK082985A-DEC 334/335 DELIVERY SYSTEM

View all 68 devices →

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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