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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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