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FDA 510(k)

ORALUMINATOR III AUTO-LIGHT

K-Number: K791771 · 1979-11-20

ApplicantMidwest
Decision Date1979-11-20
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORALUMINATOR III AUTO-LIGHT is the device name listed in this FDA 510(k) record. The listed applicant is Midwest. It received FDA 510(k) clearance on 1979-11-20 under 510(k) number K791771. The device is classified under product code EAY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORALUMINATOR III AUTO-LIGHT?

ORALUMINATOR III AUTO-LIGHT is a medical device that received FDA 510(k) clearance on 1979-11-20. The listed applicant is Midwest. The 510(k) number is K791771.

When did ORALUMINATOR III AUTO-LIGHT receive FDA 510(k) clearance?

ORALUMINATOR III AUTO-LIGHT received FDA 510(k) clearance on 1979-11-20, under 510(k) number K791771.

Who is the listed applicant for ORALUMINATOR III AUTO-LIGHT?

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

What is the FDA product code for ORALUMINATOR III AUTO-LIGHT?

The FDA product code for ORALUMINATOR III AUTO-LIGHT is EAY.

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.

Other records listing Midwest 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.

View all 13 devices →

Related Devices (Code: EAY)

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.

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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