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FDA 510(k)

LIGHT, EXAMINING, DENTAL, ULTRA VIOLET

K-Number: K770685 · 1977-04-26

ApplicantParker Laboratories, Inc.
Decision Date1977-04-26
Product CodeEAQ
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LIGHT, EXAMINING, DENTAL, ULTRA VIOLET is the device name listed in this FDA 510(k) record. The listed applicant is Parker Laboratories, Inc.. It received FDA 510(k) clearance on 1977-04-26 under 510(k) number K770685. The device is classified under product code EAQ. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LIGHT, EXAMINING, DENTAL, ULTRA VIOLET?

LIGHT, EXAMINING, DENTAL, ULTRA VIOLET is a medical device that received FDA 510(k) clearance on 1977-04-26. The listed applicant is Parker Laboratories, Inc.. The 510(k) number is K770685.

When did LIGHT, EXAMINING, DENTAL, ULTRA VIOLET receive FDA 510(k) clearance?

LIGHT, EXAMINING, DENTAL, ULTRA VIOLET received FDA 510(k) clearance on 1977-04-26, under 510(k) number K770685.

Who is the listed applicant for LIGHT, EXAMINING, DENTAL, ULTRA VIOLET?

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

What is the FDA product code for LIGHT, EXAMINING, DENTAL, ULTRA VIOLET?

The FDA product code for LIGHT, EXAMINING, DENTAL, ULTRA VIOLET is EAQ.

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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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