QUATTRO CATHETER MODEL IC4593
K-Number: K070161 · 2007-02-15
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Device Summary
Frequently Asked Questions
What is the QUATTRO CATHETER MODEL IC4593?
QUATTRO CATHETER MODEL IC4593 is a medical device that received FDA 510(k) clearance on 2007-02-15. The listed applicant is Alsius Corp.. The 510(k) number is K070161.
When did QUATTRO CATHETER MODEL IC4593 receive FDA 510(k) clearance?
QUATTRO CATHETER MODEL IC4593 received FDA 510(k) clearance on 2007-02-15, under 510(k) number K070161.
Who is the listed applicant for QUATTRO CATHETER MODEL IC4593?
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 QUATTRO CATHETER MODEL IC4593?
The FDA product code for QUATTRO CATHETER MODEL IC4593 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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