Last synced on 27 January 2023 at 11:04 pm

GARDNER TYPE BONE MARROW NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841301
510(k) Type
Traditional
Applicant
POPPER & SONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1984
Days to Decision
67 days

GARDNER TYPE BONE MARROW NEEDLE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K841301
510(k) Type
Traditional
Applicant
POPPER & SONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/5/1984
Days to Decision
67 days