QUICK STAIN WRIGHT'S GIEMSA W/BUFF
K-Number: K833677 · 1983-11-25
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Device Summary
Frequently Asked Questions
What is the QUICK STAIN WRIGHT'S GIEMSA W/BUFF?
QUICK STAIN WRIGHT'S GIEMSA W/BUFF is a medical device that received FDA 510(k) clearance on 1983-11-25. The listed applicant is J.S. Medical Assoc.. The 510(k) number is K833677.
When did QUICK STAIN WRIGHT'S GIEMSA W/BUFF receive FDA 510(k) clearance?
QUICK STAIN WRIGHT'S GIEMSA W/BUFF received FDA 510(k) clearance on 1983-11-25, under 510(k) number K833677.
Who is the listed applicant for QUICK STAIN WRIGHT'S GIEMSA W/BUFF?
The FDA 510(k) record lists J.S. Medical Assoc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for QUICK STAIN WRIGHT'S GIEMSA W/BUFF?
The FDA product code for QUICK STAIN WRIGHT'S GIEMSA W/BUFF is HYF.
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 J.S. Medical Assoc. 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: HYF)
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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