WILSON-COOK GIANTURCO-ROSCH Z-STENT AND INTRODUCER
K-Number: K941350 · 1995-03-09
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Device Summary
Frequently Asked Questions
What is the WILSON-COOK GIANTURCO-ROSCH Z-STENT AND INTRODUCER?
WILSON-COOK GIANTURCO-ROSCH Z-STENT AND INTRODUCER is a medical device that received FDA 510(k) clearance on 1995-03-09. The listed applicant is Wilson-Cook Medical, Inc.. The 510(k) number is K941350.
When did WILSON-COOK GIANTURCO-ROSCH Z-STENT AND INTRODUCER receive FDA 510(k) clearance?
WILSON-COOK GIANTURCO-ROSCH Z-STENT AND INTRODUCER received FDA 510(k) clearance on 1995-03-09, under 510(k) number K941350.
Who is the listed applicant for WILSON-COOK GIANTURCO-ROSCH Z-STENT AND INTRODUCER?
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 WILSON-COOK GIANTURCO-ROSCH Z-STENT AND INTRODUCER?
The FDA product code for WILSON-COOK GIANTURCO-ROSCH Z-STENT AND INTRODUCER 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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