DuraGraft— 510(k) DEN230002

Unknown

Marizyme, Inc.

FDA 510(k) clearance DEN230002 for DuraGraft, Unknown on 2023-10-04. Applicant: Marizyme, Inc..

Clearance details

Applicant: Marizyme, Inc.
Product code: Code QEJ
Advisory panel: Gastroenterology, Urology
Date received: 2023-01-03
Decision date: 2023-10-04
Decision: Unknown
Clearance type: Direct
Location: Jupiter, FL, US

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