PERI-GUARD PERICARDIAL PATCH-HERNIA
K-Number: K833021 · 1983-12-26
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Device Summary
Frequently Asked Questions
What is the PERI-GUARD PERICARDIAL PATCH-HERNIA?
PERI-GUARD PERICARDIAL PATCH-HERNIA is a medical device that received FDA 510(k) clearance on 1983-12-26. The listed applicant is Genetic. The 510(k) number is K833021.
When did PERI-GUARD PERICARDIAL PATCH-HERNIA receive FDA 510(k) clearance?
PERI-GUARD PERICARDIAL PATCH-HERNIA received FDA 510(k) clearance on 1983-12-26, under 510(k) number K833021.
Who is the listed applicant for PERI-GUARD PERICARDIAL PATCH-HERNIA?
The FDA 510(k) record lists Genetic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PERI-GUARD PERICARDIAL PATCH-HERNIA?
The FDA product code for PERI-GUARD PERICARDIAL PATCH-HERNIA 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.
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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