INSTANT HEMATOXYLIN
K-Number: K873107 · 1987-08-21
Advertisement
Device Summary
Frequently Asked Questions
What is the INSTANT HEMATOXYLIN?
INSTANT HEMATOXYLIN is a medical device that received FDA 510(k) clearance on 1987-08-21. The listed applicant is Shandon, Inc.. The 510(k) number is K873107.
When did INSTANT HEMATOXYLIN receive FDA 510(k) clearance?
INSTANT HEMATOXYLIN received FDA 510(k) clearance on 1987-08-21, under 510(k) number K873107.
Who is the listed applicant for INSTANT HEMATOXYLIN?
The FDA 510(k) record lists Shandon, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INSTANT HEMATOXYLIN?
The FDA product code for INSTANT 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 Shandon, 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: 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.
Advertisement