One Touch Condom with Benzocaine

FDA 510(k) K171213 · Thai Nippon Rubber Industry Public Company Limited.

Substantially Equivalent

510(k) numberK171213

Submission

Device name
One Touch Condom with Benzocaine
Applicant
Thai Nippon Rubber Industry Public Company Limited.
Bangkok, TH
Received
April 25, 2017
Decision date
January 12, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement 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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K222611Male Latex CondomsHIS · Traditional Suzhou Colour-Way New Material Co., Ltd.11/28/2022SE
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More from Rb Health (Us), LLC

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K220273Onetouch Non-paraben Lubricant GelNUC · Traditional 10/21/2022SE
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Questions and answers

When was One Touch Condom with Benzocaine cleared by the FDA?

One Touch Condom with Benzocaine (K171213) received a 510(k) decision of Substantially Equivalent on January 12, 2018, 262 days after the submission was received.

What is the product code of K171213?

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