SyntrFuge System— 510(k) K203800
Substantially EquivalentSyntr Health Technologies, Inc.
FDA 510(k) clearance K203800 for SyntrFuge System, Substantially Equivalent on 2021-07-02. Applicant: Syntr Health Technologies, Inc.. Device class: 2.
Clearance details
- Applicant
- Syntr Health Technologies, Inc.
- Product code
- Code MUU
- Device class
- Class 2
- Regulation
- 21 CFR 878.5040
- Advisory panel
- General, Plastic Surgery
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Irvine, CA, US
Recent devices under product code MUU
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