Lifestyles Zero Lubricated Latex Male Condom

FDA 510(k) K163107 · Ansell Healthcare Products, LLC

Substantially Equivalent

510(k) numberK163107

Submission

Device name
Lifestyles Zero Lubricated Latex Male Condom
Applicant
Ansell Healthcare Products, LLC
Iselin, NJ, US
Received
November 7, 2016
Decision date
January 23, 2017
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
HIS – Condom
Device class
Class II (moderate risk)
Regulation
21 CFR 884.5300
Specialty
Obstetrics/Gynecology

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Questions and answers

When was Lifestyles Zero Lubricated Latex Male Condom cleared by the FDA?

Lifestyles Zero Lubricated Latex Male Condom (K163107) received a 510(k) decision of Substantially Equivalent on January 23, 2017, 77 days after the submission was received.

What is the product code of K163107?

The FDA product code is HIS – Condom, a Class II (moderate risk) device regulated under 21 CFR 884.5300.