ProdiGI— 510(k) DEN220006

Unknown

Covidien, LLC

FDA 510(k) clearance DEN220006 for ProdiGI, Unknown on 2022-06-13. Applicant: Covidien, LLC.

Clearance details

Applicant: Covidien, LLC
Product code: Code QSW
Advisory panel: Gastroenterology, Urology
Date received: 2022-01-14
Decision date: 2022-06-13
Decision: Unknown
Clearance type: Direct
Location: Santa Clara, CA, US

View on FDA.gov ↗

Data sourced from openFDA. This site is unofficial and independent of the FDA.