Last synced on 25 April 2025 at 11:05 pm

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

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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