510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K855201Substantially Equivalent

Bard Parker Perfusion Catheter

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

K855201 is the FDA 510(k) clearance record for BARD PARKER PERFUSION CATHETER, a class II device, cleared for Bd Becton Dickinson Vacutainer Systems Preanalytic on under FDA product code DQY (Catheter, Percutaneous). FDA records list 632 510(k) clearances for Bd Becton Dickinson Vacutainer Systems Preanalytic, from to . As of , FDA records show no recalls naming K855201.

Clearance record

Decision date
Received
(123 days to decision)
Product code
DQY Catheter, Percutaneous
Regulation
21 CFR 870.1250
Device class
Class II
Review panel
Cardiovascular
Applicant
Bd Becton Dickinson Vacutainer Systems Preanalytic Mack Centre Dr., Paramus NJ
Third party review
No

Clearances, product code DQY

Trailing 12 months
13 clearances under product code DQY in the twelve months to October 2026, July 2026 the highest month at 3.
Show the numbers
Monthly 510(k) clearances under FDA product code DQY, trailing twelve months
MonthClearances
November 20250
December 20252
January 20260
February 20260
March 20261
April 20262
May 20260
June 20262
July 20263
August 20262
September 20261
October 20260