GLYCAR PERICARDIAL PATCH
K-Number: K963967 · 1997-10-31
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Device Summary
Frequently Asked Questions
What is the GLYCAR PERICARDIAL PATCH?
GLYCAR PERICARDIAL PATCH is a medical device that received FDA 510(k) clearance on 1997-10-31. The listed applicant is Glycar, Inc.. The 510(k) number is K963967.
When did GLYCAR PERICARDIAL PATCH receive FDA 510(k) clearance?
GLYCAR PERICARDIAL PATCH received FDA 510(k) clearance on 1997-10-31, under 510(k) number K963967.
Who is the listed applicant for GLYCAR PERICARDIAL PATCH?
The FDA 510(k) record lists Glycar, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GLYCAR PERICARDIAL PATCH?
The FDA product code for GLYCAR PERICARDIAL PATCH 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 Glycar, 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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