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PORTEX TUOHY EPIDURAL NEEDLE 17G, PORTEX TUOHY EPIDURAL NEEDLE 18G

Page Type
Cleared 510(K)
510(k) Number
K090261
510(k) Type
Traditional
Applicant
SMITHS MEDICAL ASD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2009
Days to Decision
87 days
Submission Type
Summary

PORTEX TUOHY EPIDURAL NEEDLE 17G, PORTEX TUOHY EPIDURAL NEEDLE 18G

Page Type
Cleared 510(K)
510(k) Number
K090261
510(k) Type
Traditional
Applicant
SMITHS MEDICAL ASD, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/1/2009
Days to Decision
87 days
Submission Type
Summary