VENTED MILLEX -GV, CATHIVEX -GV— 510(k) K133004

Name: FDA 510(k) clearance K133004
Creator: U.S. Food and Drug Administration
Published: 2014-03-27

Substantially Equivalent

Merck Millipore , Ltd.

FDA 510(k) clearance K133004 for VENTED MILLEX -GV, CATHIVEX -GV, Substantially Equivalent on 2014-03-27. Applicant: Merck Millipore , Ltd.. Device class: 2.

Clearance details

Applicant: Merck Millipore , Ltd.
Product code: Code BSN
Device class: Class 2
Regulation: 21 CFR 868.5130
Advisory panel: Anesthesiology
Date received: 2013-09-25
Decision date: 2014-03-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Temecula, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BSN

view all

K190663 — Epidural MiniFilter LUER 80369-7, Epidural MiniFilter NRFit 80369-62019-06-17
K083451 — PORTEX EPIDURAL FILTER, MODEL 100/386/010, VARIOUS STANDARD AND CUSTOM TRAYS2009-03-04
K023892 — MILLEX VV, GV, AND HV SYRINGE FILTER UNITS2003-01-17
K013988 — MILLEX GP STERILIZING FILTER UNIT, MODEL SLGP 033 R2002-04-04
K963717 — MILLEX - MP FILTER UNIT (SLMPO25SS/SLMPL25SS)1997-06-10

More clearances from Merck Millipore , Ltd.

view all

K143583 — Cathivex ¿GV filter units2015-08-11

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