INSTANT EOSIN-AQUEOUS
K-Number: K893663 · 1989-06-13
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Device Summary
Frequently Asked Questions
What is the INSTANT EOSIN-AQUEOUS?
INSTANT EOSIN-AQUEOUS is a medical device that received FDA 510(k) clearance on 1989-06-13. The listed applicant is Shandon, Inc.. The 510(k) number is K893663.
When did INSTANT EOSIN-AQUEOUS receive FDA 510(k) clearance?
INSTANT EOSIN-AQUEOUS received FDA 510(k) clearance on 1989-06-13, under 510(k) number K893663.
Who is the listed applicant for INSTANT EOSIN-AQUEOUS?
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 EOSIN-AQUEOUS?
The FDA product code for INSTANT EOSIN-AQUEOUS 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 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: 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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