DuraGraft— 510(k) DEN230002
UnknownMarizyme, Inc.
FDA 510(k) clearance DEN230002 for DuraGraft, Unknown on 2023-10-04. Applicant: Marizyme, Inc.. Device class: 2.
Clearance details
- Applicant
- Marizyme, Inc.
- Product code
- Code QEJ
- Device class
- Class 2
- Regulation
- 21 CFR 876.4100
- Advisory panel
- Gastroenterology, Urology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Jupiter, FL, US
Recent devices under product code QEJ
view allData sourced from openFDA. This site is unofficial and independent of the FDA.