Last synced on 12 July 2024 at 11:04 pm

SUBDURAL DRAINAGE CATHETER KIT, SUBDURAL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974726
510(k) Type
Traditional
Applicant
ELEKTA IMPLANTS, SA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1998
Days to Decision
90 days
Submission Type
Summary

SUBDURAL DRAINAGE CATHETER KIT, SUBDURAL CATHETER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K974726
510(k) Type
Traditional
Applicant
ELEKTA IMPLANTS, SA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/18/1998
Days to Decision
90 days
Submission Type
Summary