EOSIN Y 1% ALCOHOLIC
K-Number: K843426 · 1984-09-27
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Device Summary
Frequently Asked Questions
What is the EOSIN Y 1% ALCOHOLIC?
EOSIN Y 1% ALCOHOLIC is a medical device that received FDA 510(k) clearance on 1984-09-27. The listed applicant is Accra Laboratories, Inc.. The 510(k) number is K843426.
When did EOSIN Y 1% ALCOHOLIC receive FDA 510(k) clearance?
EOSIN Y 1% ALCOHOLIC received FDA 510(k) clearance on 1984-09-27, under 510(k) number K843426.
Who is the listed applicant for EOSIN Y 1% ALCOHOLIC?
The FDA 510(k) record lists Accra Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for EOSIN Y 1% ALCOHOLIC?
The FDA product code for EOSIN Y 1% ALCOHOLIC is HYB.
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 Accra Laboratories, 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: HYB)
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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