510(k) K140193

DUREX EMBRACE PERSONAL LUBRICANT by Reckitt Benckiser, LLC — Product Code NUC

K140193 is an FDA 510(k) premarket notification submitted by Reckitt Benckiser, LLC for the device "DUREX EMBRACE PERSONAL LUBRICANT". The FDA issued a decision of Substantially Equivalent on November 4, 2014. The device falls under product code NUC (Lubricant, Personal), a Class II device regulated under 21 CFR 884.5300. Reckitt Benckiser, LLC has at least 8 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 4, 2014
Date Received
January 27, 2014
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Lubricant, Personal
Device Class
Class II
Regulation Number
884.5300
Review Panel
OB
Submission Type

This device is a personal lubricant, for penile and/or vaginal application, intended to moisturize and lubricate, to enhance the ease and comfort of intimate sexual activity, and supplement the body's natural lubrication. This product may or may not be compatible with natural rubber latex, polyisoprene, and/or polyurethane condoms.