Last synced on 20 December 2024 at 11:05 pm

WESTERMAN-JENSEN BIOPSY NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840168
510(k) Type
Traditional
Applicant
POPPER & SONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1984
Days to Decision
56 days

WESTERMAN-JENSEN BIOPSY NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K840168
510(k) Type
Traditional
Applicant
POPPER & SONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/12/1984
Days to Decision
56 days