HARRIS HEMATOXYLIN
K-Number: K810733 · 1981-04-14
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Device Summary
Frequently Asked Questions
What is the HARRIS HEMATOXYLIN?
HARRIS HEMATOXYLIN is a medical device that received FDA 510(k) clearance on 1981-04-14. The listed applicant is Surgipath. The 510(k) number is K810733.
When did HARRIS HEMATOXYLIN receive FDA 510(k) clearance?
HARRIS HEMATOXYLIN received FDA 510(k) clearance on 1981-04-14, under 510(k) number K810733.
Who is the listed applicant for HARRIS HEMATOXYLIN?
The FDA 510(k) record lists Surgipath as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HARRIS HEMATOXYLIN?
The FDA product code for HARRIS HEMATOXYLIN is HYK.
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 Surgipath 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: HYK)
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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