PercuNav Image Fusion and Interventional Navigation System— 510(k) K223804
Substantially EquivalentPhilips Ultrasound, LLC
FDA 510(k) clearance K223804 for PercuNav Image Fusion and Interventional Navigation System, Substantially Equivalent on 2023-01-18. Applicant: Philips Ultrasound, LLC. Device class: 2.
Clearance details
- Applicant
- Philips Ultrasound, LLC
- Product code
- Code JAK
- Device class
- Class 2
- Regulation
- 21 CFR 892.1750
- Advisory panel
- Radiology
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- Bothell, WA, US
Recent devices under product code JAK
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- K260667 — Alturion Series Diagnostic Ultrasound System
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- K260680 — EPIQ Series Diagnostic Ultrasound Systems; Affiniti Series Diagnostic Ultrasound Systems
Adverse events under product code JAK
product code JAK- Death
- 27
- Injury
- 571
- Malfunction
- 779
- Total
- 1,377
Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →
Data sourced from openFDA. This site is unofficial and independent of the FDA.