Last synced on 25 November 2022 at 11:04 pm

ROTEX SCREW BIOPSY NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854404
510(k) Type
Traditional
Applicant
MEADOX SURGIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1985
Days to Decision
31 days

ROTEX SCREW BIOPSY NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K854404
510(k) Type
Traditional
Applicant
MEADOX SURGIMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/1985
Days to Decision
31 days