EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System — Philips Ultrasound, LLC (510(k) K251651)
EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System — Philips Ultrasound, LLC (510(k) K251651) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System; Applicant: Ph
| Device name | EPIQ Series Diagnostic Ultrasound System; Affiniti Series Diagnostic Ultrasound System |
|---|---|
| Applicant | Philips Ultrasound, LLC |
| Clearance track | 510(k) |
| Submission number | K251651 |
| Decision | Substantially Equivalent |
| Decision date | 2025-10-09 |
| Date received | 2025-05-29 |
| Product code | IYN |
| Device class | 2 |
| Medical specialty | Radiology |
| Applicant location | WA, US |
| Source | openFDA device |
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$1999/mo
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