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TE ME NA EPIDURAL CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991259
510(k) Type
Traditional
Applicant
Te ME NA S.A.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2001
Days to Decision
680 days
Submission Type
Statement

TE ME NA EPIDURAL CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K991259
510(k) Type
Traditional
Applicant
Te ME NA S.A.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/21/2001
Days to Decision
680 days
Submission Type
Statement