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PORTEX HYPODERMIC NEEDLE- PRO EDGE SAFETY DEVICE, 18GX1, 401810, 19GX1, 401910, 20GX1,402010, 21GX1402110

Page Type
Cleared 510(K)
510(k) Number
K063450
510(k) Type
Abbreviated
Applicant
SMITHS MEDICAL ASD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2007
Days to Decision
71 days
Submission Type
Summary

PORTEX HYPODERMIC NEEDLE- PRO EDGE SAFETY DEVICE, 18GX1, 401810, 19GX1, 401910, 20GX1,402010, 21GX1402110

Page Type
Cleared 510(K)
510(k) Number
K063450
510(k) Type
Abbreviated
Applicant
SMITHS MEDICAL ASD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2007
Days to Decision
71 days
Submission Type
Summary