WRIGHT STAIN BUFFER
K-Number: K842914 · 1984-09-07
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Device Summary
Frequently Asked Questions
What is the WRIGHT STAIN BUFFER?
WRIGHT STAIN BUFFER 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 K842914.
When did WRIGHT STAIN BUFFER receive FDA 510(k) clearance?
WRIGHT STAIN BUFFER received FDA 510(k) clearance on 1984-09-07, under 510(k) number K842914.
Who is the listed applicant for WRIGHT STAIN BUFFER?
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 BUFFER?
The FDA product code for WRIGHT STAIN BUFFER is JCC.
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: JCC)
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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