LOGIQ Vita - LOGIQ Vita
by GE Medical Systems Ultrasound and Primary Care Diagnostics
510(k) K260673
Active
Valid until
No expiry
FDA recalls
None foundDocuments
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | FDA 510(k)SESE | NumberK260673 | Date24 Mar 2026 | StatusActive |
Recalls
No FDA recalls found in the data synced 22 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — FDA 510(k) Active
Specification
- 510(k) Number
- FDA Product Code
- IYN
- Models / Variants
- LOGIQ Vita
- Device Class
- Class II
- Regulation
- 21 CFR Part 892.1550
- Advisory Committee
- Radiology
- FDA Decision
- SESE Substantially Equivalent
Overview
AI-generated summary, 6 Oct 2026
The Logiq Vita and Logiq S20 series are ultrasound systems that utilize pulsed Doppler ultrasonic technology to help clinicians visualize and assess internal body structures. These systems aid in diagnostic imaging by providing detailed ultrasound images and Doppler data, supporting assessment of blood flow and tissue structure. The device is used for ultrasound evaluation of various body structures.
The Logiq Vita and Logiq S20 series are supplied in different models, including Logiq Vita, Logiq Vita Pro, Logiq Vita Express, Logiq Vita Plus, Logiq Vita Power, Logiq S20, Logiq S20 Pro, Logiq S20 Express, Logiq S20 Plus, and Logiq S20 Power. The device has been authorized with FDA 510K clearance, with the reference number K260673.
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