WRIGHT STAIN FIXATIVE
K-Number: K842913 · 1984-09-07
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Device Summary
Frequently Asked Questions
What is the WRIGHT STAIN FIXATIVE?
WRIGHT STAIN FIXATIVE is a medical device that received FDA 510(k) clearance on 1984-09-07. The listed applicant is E K Ind., Inc.. The 510(k) number is K842913.
When did WRIGHT STAIN FIXATIVE receive FDA 510(k) clearance?
WRIGHT STAIN FIXATIVE received FDA 510(k) clearance on 1984-09-07, under 510(k) number K842913.
Who is the listed applicant for WRIGHT STAIN FIXATIVE?
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 WRIGHT STAIN FIXATIVE?
The FDA product code for WRIGHT STAIN FIXATIVE is LDZ.
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: LDZ)
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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