FDA 510(k) Applications Submitted by S&G BIOTECH INC.

FDA 510(k) Number Submission Date Device Name Applicant
K223354 11/02/2022 EGIS Biliary Single Bare Stent S&G Biotech Inc.
K242845 09/20/2024 EGIS Biliary Double Bare Stent (BDB080405) S&G BIOTECH INC.


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