510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K230865Substantially Equivalent

PIVO™ Pro Needle-free Blood Collection Device

Becton Dickinson Infusion Therapy Systems Inc., Sandy UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K230865 is the FDA 510(k) clearance record for PIVO™ Pro Needle-free Blood Collection Device, a class II device, cleared for Becton Dickinson Infusion Therapy Systems, Inc. on under FDA product code JKA (Tubes, Vials, Systems, Serum Separators, Blood Collection). FDA records list 44 510(k) clearances for Becton Dickinson Infusion Therapy Systems, Inc., from to . As of , FDA records show no recalls naming K230865.

Clearance record

Decision date
Received
(183 days to decision)
Product code
JKA Tubes, Vials, Systems, Serum Separators, Blood Collection
Regulation
21 CFR 862.1675
Device class
Class II
Review panel
Clinical Chemistry
Applicant
Becton Dickinson Infusion Therapy Systems, Inc. 9450 S. State St., Sandy UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code JKA

Trailing 12 months
6 clearances under product code JKA in the twelve months to October 2026, April 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code JKA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20263
May 20260
June 20261
July 20260
August 20260
September 20261
October 20260