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NIPRO SAFETOUCH SAFETY FISTULA NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K002813
510(k) Type
Traditional
Applicant
NIPRO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2000
Days to Decision
74 days
Submission Type
Summary

NIPRO SAFETOUCH SAFETY FISTULA NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K002813
510(k) Type
Traditional
Applicant
NIPRO MEDICAL CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/21/2000
Days to Decision
74 days
Submission Type
Summary