Last synced on 27 January 2023 at 11:04 pm

MODIFICATION TO: BD DURASAFE PLUS EPIDURAL LOCK CSE NEEDLE SET/KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012584
510(k) Type
Special
Applicant
BD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2001
Days to Decision
27 days
Submission Type
Summary

MODIFICATION TO: BD DURASAFE PLUS EPIDURAL LOCK CSE NEEDLE SET/KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K012584
510(k) Type
Special
Applicant
BD
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2001
Days to Decision
27 days
Submission Type
Summary