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MODIFICATION TO: NIPRO SAFE TOUCH SAFETY FISTULA NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K032777
510(k) Type
Special
Applicant
Nipro Medical Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2003
Days to Decision
67 days
Submission Type
Summary

MODIFICATION TO: NIPRO SAFE TOUCH SAFETY FISTULA NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K032777
510(k) Type
Special
Applicant
Nipro Medical Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/14/2003
Days to Decision
67 days
Submission Type
Summary