CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE
K-Number: K921147 · 1992-06-16
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Device Summary
Frequently Asked Questions
What is the CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE?
CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE is a medical device that received FDA 510(k) clearance on 1992-06-16. The listed applicant is Cardiovascular Imaging Systems, Inc.. The 510(k) number is K921147.
When did CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE receive FDA 510(k) clearance?
CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE received FDA 510(k) clearance on 1992-06-16, under 510(k) number K921147.
Who is the listed applicant for CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE?
The FDA 510(k) record lists Cardiovascular Imaging Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE?
The FDA product code for CVIS INSIGHT IMAGING CATHETER FOR INTRALUMINAL USE is ITX.
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 Cardiovascular Imaging Systems, 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: ITX)
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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