MobileDiagnost M50— 510(k) K173187

Substantially Equivalent

Philips India Limited

FDA 510(k) clearance K173187 for MobileDiagnost M50, Substantially Equivalent on 2017-11-16. Applicant: Philips India Limited.

Clearance details

Applicant: Philips India Limited
Product code: Code IZL
Advisory panel: Radiology
Date received: 2017-10-02
Decision date: 2017-11-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Pune, IN

Download summary PDF View on FDA.gov ↗

Adverse events under product code IZL

product code IZL

Other: 3
Total: 3

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. 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.