SilverCoat Silicone Foley Catheter

FDA 510(k) K150550 · Covalontechnologies, Inc.

Substantially Equivalent

510(k) numberK150550

Submission

Device name
SilverCoat Silicone Foley Catheter
Applicant
Covalontechnologies, Inc.
Mississauga, CA
Received
March 3, 2015
Decision date
November 24, 2015
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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Questions and answers

When was SilverCoat Silicone Foley Catheter cleared by the FDA?

SilverCoat Silicone Foley Catheter (K150550) received a 510(k) decision of Substantially Equivalent on November 24, 2015, 266 days after the submission was received.

What is the product code of K150550?

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