HEMATOXYLIN
K-Number: K811802 · 1981-07-28
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Device Summary
Frequently Asked Questions
What is the HEMATOXYLIN?
HEMATOXYLIN is a medical device that received FDA 510(k) clearance on 1981-07-28. The listed applicant is Richard-Allan Medical Ind., Inc.. The 510(k) number is K811802.
When did HEMATOXYLIN receive FDA 510(k) clearance?
HEMATOXYLIN received FDA 510(k) clearance on 1981-07-28, under 510(k) number K811802.
Who is the listed applicant for HEMATOXYLIN?
The FDA 510(k) record lists Richard-Allan Medical Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HEMATOXYLIN?
The FDA product code for HEMATOXYLIN is HYJ.
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 Richard-Allan Medical 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: HYJ)
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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