PATCH, PLEDGET AND INTRACARDIAC
K-Number: K111187 · 2011-07-26
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Device Summary
Frequently Asked Questions
What is the PATCH, PLEDGET AND INTRACARDIAC?
PATCH, PLEDGET AND INTRACARDIAC is a medical device that received FDA 510(k) clearance on 2011-07-26. The listed applicant is Cormatrix Cardiovascular, Inc.. The 510(k) number is K111187.
When did PATCH, PLEDGET AND INTRACARDIAC receive FDA 510(k) clearance?
PATCH, PLEDGET AND INTRACARDIAC received FDA 510(k) clearance on 2011-07-26, under 510(k) number K111187.
Who is the listed applicant for PATCH, PLEDGET AND INTRACARDIAC?
The FDA 510(k) record lists Cormatrix Cardiovascular, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PATCH, PLEDGET AND INTRACARDIAC?
The FDA product code for PATCH, PLEDGET AND INTRACARDIAC is DXZ.
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 Cormatrix Cardiovascular, 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: DXZ)
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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