510(K) CLEARANCES 49 ▼18RECALLS POSTED 23 ▼3CLASS I 1 ▼1PMA DECISIONS 37 ▼3WEEK ENDING / FDA DATA AS OF
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K885221Substantially Equivalent

Multilumen Central Venous Catheter

BD Becton Dickinson Vacutainer Systems Preanalytic, Sandy UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K885221 is the FDA 510(k) clearance record for MULTILUMEN CENTRAL VENOUS CATHETER, a class II device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code DQO (Catheter, Intravascular, Diagnostic). FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show no recalls naming K885221.

Clearance record

Decision date
Received
(373 days to decision)
Product code
DQO Catheter, Intravascular, Diagnostic
Regulation
21 CFR 870.1200
Device class
Class II
Review panel
Cardiovascular
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic 9450 S. State Sreet, Sandy UT
Third party review
No

Clearances, product code DQO

Trailing 12 months
3 clearances under product code DQO in the twelve months to November 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code DQO, trailing twelve months
MonthClearances
December 20250
January 20260
February 20260
March 20261
April 20260
May 20261
June 20261
July 20260
August 20260
September 20260
October 20260
November 20260