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NIPRO BIOHOLE NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K063368
510(k) Type
Traditional
Applicant
Nipro Medical Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2007
Days to Decision
90 days
Submission Type
Summary

NIPRO BIOHOLE NEEDLE

Page Type
Cleared 510(K)
510(k) Number
K063368
510(k) Type
Traditional
Applicant
Nipro Medical Corp.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/2007
Days to Decision
90 days
Submission Type
Summary