EG-3630UR— 510(k) K041395

Substantially Equivalent

Pentax Precision Instrument Corp.

FDA 510(k) clearance K041395 for EG-3630UR, Substantially Equivalent on 2004-06-09. Applicant: Pentax Precision Instrument Corp..

Clearance details

Applicant: Pentax Precision Instrument Corp.
Product code: Code ITX
Advisory panel: Radiology
Date received: 2004-05-26
Decision date: 2004-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Orangeburg, NY, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code ITX

product code ITX

Death: 6
Injury: 137
Malfunction: 2,036
Total: 2,179

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.