SOEHENDRA STENT RETRIEVER
K-Number: K903420 · 1990-10-22
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Device Summary
Frequently Asked Questions
What is the SOEHENDRA STENT RETRIEVER?
SOEHENDRA STENT RETRIEVER is a medical device that received FDA 510(k) clearance on 1990-10-22. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K903420.
When did SOEHENDRA STENT RETRIEVER receive FDA 510(k) clearance?
SOEHENDRA STENT RETRIEVER received FDA 510(k) clearance on 1990-10-22, under 510(k) number K903420.
Who is the listed applicant for SOEHENDRA STENT RETRIEVER?
The FDA 510(k) record lists Wilson-Cook Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOEHENDRA STENT RETRIEVER?
The FDA product code for SOEHENDRA STENT RETRIEVER is FGE.
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 Wilson-Cook Medical, 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: FGE)
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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