INTERCEPTOR PLUS CORONARY FILTER SYSTEMS
K-Number: K073523 · 2008-08-01
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Device Summary
Frequently Asked Questions
What is the INTERCEPTOR PLUS CORONARY FILTER SYSTEMS?
INTERCEPTOR PLUS CORONARY FILTER SYSTEMS is a medical device that received FDA 510(k) clearance on 2008-08-01. The listed applicant is Medtronic, Inc.. The 510(k) number is K073523.
When did INTERCEPTOR PLUS CORONARY FILTER SYSTEMS receive FDA 510(k) clearance?
INTERCEPTOR PLUS CORONARY FILTER SYSTEMS received FDA 510(k) clearance on 2008-08-01, under 510(k) number K073523.
Who is the listed applicant for INTERCEPTOR PLUS CORONARY FILTER SYSTEMS?
The FDA 510(k) record lists Medtronic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTERCEPTOR PLUS CORONARY FILTER SYSTEMS?
The FDA product code for INTERCEPTOR PLUS CORONARY FILTER SYSTEMS is NFA.
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 Medtronic, 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: NFA)
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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