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FDA 510(k)

ORALUMINATOR III - LIGHT SOURCE FOR F.O.

K-Number: K760796 · 1976-10-20

ApplicantMidwest
Decision Date1976-10-20
Product CodeEAY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ORALUMINATOR III - LIGHT SOURCE FOR F.O. is the device name listed in this FDA 510(k) record. The listed applicant is Midwest. It received FDA 510(k) clearance on 1976-10-20 under 510(k) number K760796. 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 - LIGHT SOURCE FOR F.O.?

ORALUMINATOR III - LIGHT SOURCE FOR F.O. is a medical device that received FDA 510(k) clearance on 1976-10-20. The listed applicant is Midwest. The 510(k) number is K760796.

When did ORALUMINATOR III - LIGHT SOURCE FOR F.O. receive FDA 510(k) clearance?

ORALUMINATOR III - LIGHT SOURCE FOR F.O. received FDA 510(k) clearance on 1976-10-20, under 510(k) number K760796.

Who is the listed applicant for ORALUMINATOR III - LIGHT SOURCE FOR F.O.?

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 - LIGHT SOURCE FOR F.O.?

The FDA product code for ORALUMINATOR III - LIGHT SOURCE FOR F.O. is EAY.

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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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