ULTRASOUND VIDEO BRONCHOSCOPE, MODEL EB-1970UK— 510(k) K081518

Substantially Equivalent

Pentax Medical Company

FDA 510(k) clearance K081518 for ULTRASOUND VIDEO BRONCHOSCOPE, MODEL EB-1970UK, Substantially Equivalent on 2008-09-05. Applicant: Pentax Medical Company.

Clearance details

Applicant: Pentax Medical Company
Product code: Code EOQ
Advisory panel: Ear, Nose, Throat
Date received: 2008-05-30
Decision date: 2008-09-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Montvale, NJ, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code EOQ

product code EOQ

Death: 135
Injury: 2,863
Malfunction: 21,662
Total: 24,660

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.