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Biowy PlCC Catheter

Page Type
Cleared 510(K)
510(k) Number
K173956
510(k) Type
Traditional
Applicant
Biowy Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2018
Days to Decision
144 days
Submission Type
Summary

Biowy PlCC Catheter

Page Type
Cleared 510(K)
510(k) Number
K173956
510(k) Type
Traditional
Applicant
Biowy Corporation
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/21/2018
Days to Decision
144 days
Submission Type
Summary