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FDA 510(k)

PRESERV GOMORI TRICHROME STAIN 125/500

K-Number: K840087 · 1984-02-10

ApplicantPreventive Diagnostics Corp.
Decision Date1984-02-10
Product CodeLED
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

PRESERV GOMORI TRICHROME STAIN 125/500 is the device name listed in this FDA 510(k) record. The listed applicant is Preventive Diagnostics Corp.. It received FDA 510(k) clearance on 1984-02-10 under 510(k) number K840087. The device is classified under product code LED. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRESERV GOMORI TRICHROME STAIN 125/500?

PRESERV GOMORI TRICHROME STAIN 125/500 is a medical device that received FDA 510(k) clearance on 1984-02-10. The listed applicant is Preventive Diagnostics Corp.. The 510(k) number is K840087.

When did PRESERV GOMORI TRICHROME STAIN 125/500 receive FDA 510(k) clearance?

PRESERV GOMORI TRICHROME STAIN 125/500 received FDA 510(k) clearance on 1984-02-10, under 510(k) number K840087.

Who is the listed applicant for PRESERV GOMORI TRICHROME STAIN 125/500?

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

What is the FDA product code for PRESERV GOMORI TRICHROME STAIN 125/500?

The FDA product code for PRESERV GOMORI TRICHROME STAIN 125/500 is LED.

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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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