510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K111366Substantially Equivalent

Bd Nexiva Diffusics Closed IV Catheter System

Becton, Dickinson & Company (BD), Sandy UT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K111366 is the FDA 510(k) clearance record for BD NEXIVA DIFFUSICS CLOSED IV CATHETER SYSTEM, a class II device, cleared for Becton, Dickinson and Company (BD) on under FDA product code FOZ (Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days). FDA records list 5 510(k) clearances for Becton, Dickinson and Company (BD), from to . As of , FDA records show no recalls naming K111366.

Clearance record

Decision date
Received
(137 days to decision)
Product code
FOZ Catheter, Intravascular, Therapeutic, Short-Term Less Than 30 Days
Regulation
21 CFR 880.5200
Device class
Class II
Review panel
General Hospital
Applicant
Becton, Dickinson and Company (BD) 9450 S. State St., Sandy UT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FOZ

Trailing 12 months
9 clearances under product code FOZ in the twelve months to October 2026, April 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FOZ, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20260
April 20262
May 20261
June 20260
July 20262
August 20261
September 20261
October 20260