WRIGHT-GIEMSA QUICK STAIN
K-Number: K842745 · 1984-08-10
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Device Summary
Frequently Asked Questions
What is the WRIGHT-GIEMSA QUICK STAIN?
WRIGHT-GIEMSA QUICK STAIN is a medical device that received FDA 510(k) clearance on 1984-08-10. The listed applicant is E K Ind., Inc.. The 510(k) number is K842745.
When did WRIGHT-GIEMSA QUICK STAIN receive FDA 510(k) clearance?
WRIGHT-GIEMSA QUICK STAIN received FDA 510(k) clearance on 1984-08-10, under 510(k) number K842745.
Who is the listed applicant for WRIGHT-GIEMSA QUICK 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 WRIGHT-GIEMSA QUICK STAIN?
The FDA product code for WRIGHT-GIEMSA QUICK STAIN is IAF.
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: IAF)
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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