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Biowy Corporation
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K233658
Biowy Tym Tube (TT)
February 16, 2024
K192246
Biowy PICC Catheter S Kit
April 30, 2020
K173956
Biowy PlCC Catheter
May 21, 2018