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CAREFINE PEN NEEDLE FAMILY INCLUDING QUINTAPOINT AND SUPERPOINT

Page Type
Cleared 510(K)
510(k) Number
K141749
510(k) Type
Special
Applicant
FACET TECHNOLOGIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2014
Days to Decision
29 days
Submission Type
Summary

CAREFINE PEN NEEDLE FAMILY INCLUDING QUINTAPOINT AND SUPERPOINT

Page Type
Cleared 510(K)
510(k) Number
K141749
510(k) Type
Special
Applicant
FACET TECHNOLOGIES, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2014
Days to Decision
29 days
Submission Type
Summary