INVIDOS— 510(k) K002051

Substantially Equivalent

Scanditronix Medical AB

FDA 510(k) clearance K002051 for INVIDOS, Substantially Equivalent on 2000-09-05. Applicant: Scanditronix Medical AB.

Clearance details

Applicant: Scanditronix Medical AB
Product code: Code IYE
Advisory panel: Radiology
Date received: 2000-07-06
Decision date: 2000-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Uppsala S-754 50, SE

Download summary PDF View on FDA.gov ↗

Adverse events under product code IYE

product code IYE

Malfunction: 455
Other: 3
Total: 458

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.