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FDA 510(k)

BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes

K-Number: K252040 · 2026-03-13

Decision Date2026-03-13
Product CodeJKA
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes is a medical device manufactured by Becton, Dickinson and Company. It received FDA 510(k) clearance on 2026-03-13 under approval number K252040. The device is classified under product code JKA. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes?

BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes is a medical device that received FDA 510(k) clearance on 2026-03-13. It is manufactured by Becton, Dickinson and Company. The 510(k) number is K252040.

When was BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes approved by the FDA?

BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes received FDA 510(k) clearance on 2026-03-13, under approval number K252040.

What company makes BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes?

BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes is manufactured by Becton, Dickinson and Company.

What is the FDA product code for BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes?

The FDA product code for BD Vacutainer® Plasma Separator Tubes (PST™), BD Vacutainer® Sodium Heparin Blood Collection Tubes is JKA.

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Official Source

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