Submission Details
| 510(k) Number | K220043 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 05, 2022 |
| Decision Date | April 05, 2022 |
| Days to Decision | 90 days |
| Submission Type | Traditional |
| Review Panel | Radiology (RA) |
| Summary | Summary PDF |
K220043 is an FDA 510(k) clearance for the HERA W10 Diagnostic Ultrasound System, HERA W9 Diagnostic Ultrasound System, a System, Imaging, Pulsed Doppler, Ultrasonic (Class II — Special Controls, product code IYN), submitted by Samsung Medison Co., Ltd. (Hongcheon-Gun, KR). The FDA issued a Cleared decision on April 5, 2022, 90 days after receiving the submission on January 5, 2022. This device falls under the Radiology review panel. Regulated under 21 CFR 892.1550.
| 510(k) Number | K220043 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | January 05, 2022 |
| Decision Date | April 05, 2022 |
| Days to Decision | 90 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 |