BioTraceIO Vision (V1.7)— 510(k) K251931
Substantially EquivalentTechsomed Medical Technologies
FDA 510(k) clearance K251931 for BioTraceIO Vision (V1.7), Substantially Equivalent on 2025-09-08. Applicant: Techsomed Medical Technologies. Device class: 2.
Clearance details
- Applicant
- Techsomed Medical Technologies
- Product code
- Code QTZ
- Device class
- Class 2
- Regulation
- 21 CFR 892.2050
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Or Yehuda, IL
Recent devices under product code QTZ
view allData sourced from openFDA. This site is unofficial and independent of the FDA.