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FDA 510(k)

RITTER STARLIGHT DENTAL OPERATING LIGHT

K-Number: K760707 · 1976-10-05

ApplicantRitter Co.
Decision Date1976-10-05
Product CodeEAZ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

RITTER STARLIGHT DENTAL OPERATING LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Ritter Co.. It received FDA 510(k) clearance on 1976-10-05 under 510(k) number K760707. 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 RITTER STARLIGHT DENTAL OPERATING LIGHT?

RITTER STARLIGHT DENTAL OPERATING LIGHT is a medical device that received FDA 510(k) clearance on 1976-10-05. The listed applicant is Ritter Co.. The 510(k) number is K760707.

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

RITTER STARLIGHT DENTAL OPERATING LIGHT received FDA 510(k) clearance on 1976-10-05, under 510(k) number K760707.

Who is the listed applicant for RITTER STARLIGHT DENTAL OPERATING LIGHT?

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

What is the FDA product code for RITTER STARLIGHT DENTAL OPERATING LIGHT?

The FDA product code for RITTER STARLIGHT DENTAL OPERATING LIGHT is EAZ.

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Other records listing Ritter Co. 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.

K831245TAYLOR PRINTER/AUTO INFLAT-SPHYGMOMANOK832171SELF CHECK DIGITAL BLOOD PRESS. MONITORK831976POWER OPTICK823180SA-21 DENTAL UNITK800084RITTER MODEL J DENTAL CHAIRK781101ELECTROSURGICAL UNIT 75

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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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