ORALUMINATOR III AUTO-LIGHT
K-Number: K791771 · 1979-11-20
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Device Summary
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.
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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