GILL'S HEMATOXYLIN #1
K-Number: K810758 · 1981-04-14
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Device Summary
Frequently Asked Questions
What is the GILL'S HEMATOXYLIN #1?
GILL'S HEMATOXYLIN #1 is a medical device that received FDA 510(k) clearance on 1981-04-14. The listed applicant is Surgipath. The 510(k) number is K810758.
When did GILL'S HEMATOXYLIN #1 receive FDA 510(k) clearance?
GILL'S HEMATOXYLIN #1 received FDA 510(k) clearance on 1981-04-14, under 510(k) number K810758.
Who is the listed applicant for GILL'S HEMATOXYLIN #1?
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 GILL'S HEMATOXYLIN #1?
The FDA product code for GILL'S HEMATOXYLIN #1 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 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: 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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