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FDA 510(k)

DENTAL LAMP HANDLE COVER

K-Number: K884223 · 1989-03-17

ApplicantSteri-Shield Products, Inc.
Decision Date1989-03-17
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

DENTAL LAMP HANDLE COVER is the device name listed in this FDA 510(k) record. The listed applicant is Steri-Shield Products, Inc.. It received FDA 510(k) clearance on 1989-03-17 under 510(k) number K884223. 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 LAMP HANDLE COVER?

DENTAL LAMP HANDLE COVER is a medical device that received FDA 510(k) clearance on 1989-03-17. The listed applicant is Steri-Shield Products, Inc.. The 510(k) number is K884223.

When did DENTAL LAMP HANDLE COVER receive FDA 510(k) clearance?

DENTAL LAMP HANDLE COVER received FDA 510(k) clearance on 1989-03-17, under 510(k) number K884223.

Who is the listed applicant for DENTAL LAMP HANDLE COVER?

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

What is the FDA product code for DENTAL LAMP HANDLE COVER?

The FDA product code for DENTAL LAMP HANDLE COVER is EAZ.

Related Clinical Trials

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.

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Other records listing Steri-Shield Products, 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.

K884220AIR WATER SYRINGE TIP SHIELDK884219BRACKET TABLE ARM COVERK884221ULTRASONIC SCALER COVERK884222CURING LIGHT COVER

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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