SOLEX CATHETER, MODEL SL2593
K-Number: K081936 · 2008-08-13
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Device Summary
Frequently Asked Questions
What is the SOLEX CATHETER, MODEL SL2593?
SOLEX CATHETER, MODEL SL2593 is a medical device that received FDA 510(k) clearance on 2008-08-13. The listed applicant is Alsius Corp.. The 510(k) number is K081936.
When did SOLEX CATHETER, MODEL SL2593 receive FDA 510(k) clearance?
SOLEX CATHETER, MODEL SL2593 received FDA 510(k) clearance on 2008-08-13, under 510(k) number K081936.
Who is the listed applicant for SOLEX CATHETER, MODEL SL2593?
The FDA 510(k) record lists Alsius Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for SOLEX CATHETER, MODEL SL2593?
The FDA product code for SOLEX CATHETER, MODEL SL2593 is NCX.
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 Alsius Corp. 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: NCX)
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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