MEDTRADE PRODUCTS ALGINATE ISLAND
K-Number: K000487 · 2000-04-18
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Device Summary
Frequently Asked Questions
What is the MEDTRADE PRODUCTS ALGINATE ISLAND?
MEDTRADE PRODUCTS ALGINATE ISLAND is a medical device that received FDA 510(k) clearance on 2000-04-18. The listed applicant is Medtrade Products , Ltd.. The 510(k) number is K000487.
When did MEDTRADE PRODUCTS ALGINATE ISLAND receive FDA 510(k) clearance?
MEDTRADE PRODUCTS ALGINATE ISLAND received FDA 510(k) clearance on 2000-04-18, under 510(k) number K000487.
Who is the listed applicant for MEDTRADE PRODUCTS ALGINATE ISLAND?
The FDA 510(k) record lists Medtrade Products , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDTRADE PRODUCTS ALGINATE ISLAND?
The FDA product code for MEDTRADE PRODUCTS ALGINATE ISLAND is KGN.
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 Medtrade Products , Ltd. 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: KGN)
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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