FDA 510(k) Applications Submitted by Integrated Endoscopy, Inc.

FDA 510(k) Number Submission Date Device Name Applicant
K191594 06/17/2019 Nuvis Battery Arthroscope Integrated Endoscopy, Inc.
K140903 04/09/2014 NUVIS ARTHROSCOPE INTEGRATED ENDOSCOPY, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact