Option-Vm Urinary Catheter/Adpater, Models MV39016, MVA39016

FDA 510(k) K041983 · Opticon Medical

Substantially Equivalent

510(k) numberK041983

Submission

Device name
Option-Vm Urinary Catheter/Adpater, Models MV39016, MVA39016
Applicant
Opticon Medical
Dublin, OH, US
Received
July 23, 2004
Decision date
November 17, 2004
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
EZL – Catheter, Retention Type, Balloon
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5130
Specialty
Gastroenterology, Urology

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More from Teleflexmedical, Inc.

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K033830Option-Vf Urinary Catheter with Adaptor, Model FVA14218; Option-V Continuous Drainage…EZL · Special 01/09/2004SE
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K970716Opticon Direct Male Urinary Catheter for Continuous DrainageEZL · Traditional 05/16/1997SE
K930194Hemostasis Valve and Tubing SetDYB · Traditional 09/22/1993SE
K904999Weingarten TM Capnographic Intubation StyletteBSR · Traditional 01/26/1993SE
K895955Loper Celiac Plexus Block Catheter KitCAZ · Traditional 02/22/1990SE
K895476Option Epidural CathetersCAZ · Traditional 01/19/1990SE

Questions and answers

When was Option-Vm Urinary Catheter/Adpater, Models MV39016, MVA39016 cleared by the FDA?

Option-Vm Urinary Catheter/Adpater, Models MV39016, MVA39016 (K041983) received a 510(k) decision of Substantially Equivalent on November 17, 2004, 117 days after the submission was received.

What is the product code of K041983?

The FDA product code is EZL – Catheter, Retention Type, Balloon, a Class II (moderate risk) device regulated under 21 CFR 876.5130.