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Kendall NPWT Incision Management Device

Page Type
Cleared 510(K)
510(k) Number
K202217
510(k) Type
Traditional
Applicant
Cardinal Health
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2021
Days to Decision
302 days
Submission Type
Summary

Kendall NPWT Incision Management Device

Page Type
Cleared 510(K)
510(k) Number
K202217
510(k) Type
Traditional
Applicant
Cardinal Health
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/4/2021
Days to Decision
302 days
Submission Type
Summary