BD Acute Central Line— 510(k) K190855

Name: FDA 510(k) clearance K190855
Creator: U.S. Food and Drug Administration
Published: 2019-11-01

Substantially Equivalent

Bard Access Systems, Inc. (Bard Has Joined Bd)

FDA 510(k) clearance K190855 for BD Acute Central Line, Substantially Equivalent on 2019-11-01. Applicant: Bard Access Systems, Inc. (Bard Has Joined Bd). Device class: 2.

Clearance details

Applicant: Bard Access Systems, Inc. (Bard Has Joined Bd)
Product code: Code FOZ
Device class: Class 2
Regulation: 21 CFR 880.5200
Advisory panel: General Hospital
Date received: 2019-04-02
Decision date: 2019-11-01
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake Ciy,, UT, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FOZ

view all

K260432 — Ruby Intravascular Catheter2026-09-02
K260165 — Unimpregnated Central Venous Catheter2026-08-10
K261041 — ClearSafe Closed System2026-07-10
K260539 — MedSource QuickSafe Safety IV Catheter; MedSource PurSafe Safety IV Catheter2026-07-09
K253235 — Introcan Safety® Deep Access XL IV Catheter2026-05-15

More clearances from Bard Access Systems, Inc. (Bard Has Joined Bd)

view all

K200266 — BD Centro Vena Acute Central Line (7 French Dual Lumen)2020-04-07

Adverse events under product code FOZ

product code FOZ

Death: 38
Injury: 2,290
Malfunction: 25,858
Other: 11
Total: 28,197

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.