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Kendall NPWT Incision Management Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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