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SPINAL EPIDURAL NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002405
510(k) Type
Traditional
Applicant
TE ME NA S.A.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2001
Days to Decision
298 days
Submission Type
Summary

SPINAL EPIDURAL NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002405
510(k) Type
Traditional
Applicant
TE ME NA S.A.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/1/2001
Days to Decision
298 days
Submission Type
Summary