FDA 510(k)

DUAL LAB-LITE LIGHT BOX

K-Number: K771486 · 1977-08-22

Decision Date1977-08-22

Product CodeDJS

Advisory CommitteeCH

DecisionSubstantially Equivalent

Device Summary

DUAL LAB-LITE LIGHT BOX is the device name listed in this FDA 510(k) record. The listed applicant is Technilab. It received FDA 510(k) clearance on 1977-08-22 under 510(k) number K771486. The device is classified under product code DJS. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DUAL LAB-LITE LIGHT BOX?

DUAL LAB-LITE LIGHT BOX is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Technilab. The 510(k) number is K771486.

When did DUAL LAB-LITE LIGHT BOX receive FDA 510(k) clearance?

DUAL LAB-LITE LIGHT BOX received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771486.

Who is the listed applicant for DUAL LAB-LITE LIGHT BOX?

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

What is the FDA product code for DUAL LAB-LITE LIGHT BOX?

The FDA product code for DUAL LAB-LITE LIGHT BOX is DJS.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.