Cala kIQ— 510(k) K242259
Substantially EquivalentCala Health, Inc.
FDA 510(k) clearance K242259 for Cala kIQ, Substantially Equivalent on 2024-11-22. Applicant: Cala Health, Inc.. Device class: 2.
Clearance details
- Applicant
- Cala Health, Inc.
- Product code
- Code QBC
- Device class
- Class 2
- Regulation
- 21 CFR 882.5897
- Advisory panel
- Neurology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- San Mateo, CA, US
Recent devices under product code QBC
view allMore clearances from Cala Health, Inc.
view allData sourced from openFDA. This site is unofficial and independent of the FDA.