LIA Console (542-7)— 510(k) K251730
Substantially EquivalentLeadoptik, Inc.
FDA 510(k) clearance K251730 for LIA Console (542-7), Substantially Equivalent on 2025-12-19. Applicant: Leadoptik, Inc.. Device class: 2.
Clearance details
- Applicant
- Leadoptik, Inc.
- Product code
- Code NQQ
- Device class
- Class 2
- Regulation
- 21 CFR 892.1560
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Jose, CA, US
Recent devices under product code NQQ
view allMore clearances from Leadoptik, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.