QIKCAP System— 510(k) DEN250004
UnknownHai Solutions
FDA 510(k) clearance DEN250004 for QIKCAP System, Unknown on 2025-12-23. Applicant: Hai Solutions. Device class: 2.
Clearance details
- Applicant
- Hai Solutions
- Product code
- Code SGX
- Device class
- Class 2
- Regulation
- 21 CFR 880.6512
- Advisory panel
- General Hospital
- Date received
- Decision date
- Decision
- Unknown
- Clearance type
- Direct
- Location
- Carlsbad, CA, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.