SENTINEL, MODEL SP-001— 510(k) K082582

Substantially Equivalent

C-Rad Positioning AB

FDA 510(k) clearance K082582 for SENTINEL, MODEL SP-001, Substantially Equivalent on 2009-03-30. Applicant: C-Rad Positioning AB.

Clearance details

Applicant: C-Rad Positioning AB
Product code: Code IYE
Advisory panel: Radiology
Date received: 2008-09-08
Decision date: 2009-03-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Uppsala, 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.