Last synced on 9 May 2025 at 11:05 pm

MANUAL-BONE-MARROW-BIOPSY-NEEDLES, SEMI-AUTOMATIC-BIOPSY-NEEDLES, AUTOMATIC-BIOPSY-NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130616
510(k) Type
Traditional
Applicant
BIOPSYBELL S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2014
Days to Decision
337 days
Submission Type
Summary

MANUAL-BONE-MARROW-BIOPSY-NEEDLES, SEMI-AUTOMATIC-BIOPSY-NEEDLES, AUTOMATIC-BIOPSY-NEEDLES

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130616
510(k) Type
Traditional
Applicant
BIOPSYBELL S.R.L.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/7/2014
Days to Decision
337 days
Submission Type
Summary