GOMORI'S TRICHROME STAIN
K-Number: K842930 · 1984-09-11
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Device Summary
Frequently Asked Questions
What is the GOMORI'S TRICHROME STAIN?
GOMORI'S TRICHROME STAIN is a medical device that received FDA 510(k) clearance on 1984-09-11. The listed applicant is E K Ind., Inc.. The 510(k) number is K842930.
When did GOMORI'S TRICHROME STAIN receive FDA 510(k) clearance?
GOMORI'S TRICHROME STAIN received FDA 510(k) clearance on 1984-09-11, under 510(k) number K842930.
Who is the listed applicant for GOMORI'S TRICHROME STAIN?
The FDA 510(k) record lists E K Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GOMORI'S TRICHROME STAIN?
The FDA product code for GOMORI'S TRICHROME STAIN is LED.
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 E K Ind., Inc. 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: LED)
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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