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0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K000632
510(k) Type
Traditional
Applicant
Avitro, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2000
Days to Decision
238 days
Submission Type
Summary

0.9% SODIUM CHLORIDE VASCULAT ACCESS DEVICE

Page Type
Cleared 510(K)
510(k) Number
K000632
510(k) Type
Traditional
Applicant
Avitro, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/19/2000
Days to Decision
238 days
Submission Type
Summary