Last synced on 25 April 2025 at 11:05 pm

PIVO™ Pro Needle-free Blood Collection Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241586
510(k) Type
Traditional
Applicant
Becton Dickinson Infusion Therapy Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2025
Days to Decision
269 days
Submission Type
Summary

PIVO™ Pro Needle-free Blood Collection Device

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K241586
510(k) Type
Traditional
Applicant
Becton Dickinson Infusion Therapy Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/27/2025
Days to Decision
269 days
Submission Type
Summary