Submission Details
| 510(k) Number | K242005 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 09, 2024 |
| Decision Date | October 02, 2024 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
K242005 is an FDA 510(k) clearance for the Versana Premier; Versana Premier Lotus; LOGIQ F, a System, Imaging, Pulsed Doppler, Ultrasonic (Class II — Special Controls, product code IYN), submitted by GE Medical Systems Ultrasound and Primary Care Diagnostics (Waukesha, US). The FDA issued a Cleared decision on October 2, 2024, 85 days after receiving the submission on July 9, 2024. This device falls under the Radiology review panel. Regulated under 21 CFR 892.1550.
| 510(k) Number | K242005 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | July 09, 2024 |
| Decision Date | October 02, 2024 |
| Days to Decision | 85 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
| Product Code | IYN — System, Imaging, Pulsed Doppler, Ultrasonic |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 892.1550 |