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PERIFIX SAFETY EPIDURAL NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013610
510(k) Type
Traditional
Applicant
B. BRAUN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2002
Days to Decision
81 days
Submission Type
Summary

PERIFIX SAFETY EPIDURAL NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K013610
510(k) Type
Traditional
Applicant
B. BRAUN MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/25/2002
Days to Decision
81 days
Submission Type
Summary