AN5150 AND AN7150 DIGITAL RADIOLOGY SYSTEMS— 510(k) K033345

Substantially Equivalent

Analogic Corp.

FDA 510(k) clearance K033345 for AN5150 AND AN7150 DIGITAL RADIOLOGY SYSTEMS, Substantially Equivalent on 2003-11-19. Applicant: Analogic Corp..

Clearance details

Applicant: Analogic Corp.
Product code: Code KPR
Advisory panel: Radiology
Date received: 2003-10-20
Decision date: 2003-11-19
Decision: Substantially Equivalent
Clearance type: Special
Location: Peabody, MA, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KPR

product code KPR

Other: 6
Total: 6

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.