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the POWERWAND Safety Introducer with an Extended Dwell Catheter, 3Fr. Model

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162322
510(k) Type
Traditional
Applicant
ACCESS SCIENTIFIC, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2016
Days to Decision
90 days
Submission Type
Summary

the POWERWAND Safety Introducer with an Extended Dwell Catheter, 3Fr. Model

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K162322
510(k) Type
Traditional
Applicant
ACCESS SCIENTIFIC, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2016
Days to Decision
90 days
Submission Type
Summary