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Nipro SafeTouch IV Catheter

Page Type
Cleared 510(K)
510(k) Number
K161681
510(k) Type
Traditional
Applicant
NIPRO MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2017
Days to Decision
264 days
Submission Type
Summary

Nipro SafeTouch IV Catheter

Page Type
Cleared 510(K)
510(k) Number
K161681
510(k) Type
Traditional
Applicant
NIPRO MEDICAL CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/8/2017
Days to Decision
264 days
Submission Type
Summary