Procise IFX— 510(k) DEN210056
UnknownProcisedx, Inc.
FDA 510(k) clearance DEN210056 for Procise IFX, Unknown on 2023-09-29. Applicant: Procisedx, Inc.. Device class: 2.
Clearance details
- Applicant
- Procisedx, Inc.
- Product code
- Code QXT
- Device class
- Class 2
- Regulation
- 21 CFR 862.3115
- Advisory panel
- Clinical Toxicology
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- San Diego, CA, US
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