FDA 510(k) Applications Submitted by Biowy Corporation

FDA 510(k) Number Submission Date Device Name Applicant
K173956 12/28/2017 Biowy PlCC Catheter Biowy Corporation
K192246 08/19/2019 Biowy PICC Catheter S Kit Biowy Corporation


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