510(k) K122477
K122477 is an FDA 510(k) premarket notification submitted by Ansell Healthcare Products, LLC for the device "LIFESTYLES LUXE PREMIUM PERSONAL LUBRICANT". The FDA issued a decision of Substantially Equivalent on February 19, 2013. The device falls under product code NUC (Lubricant, Personal), a Class II device regulated under 21 CFR 884.5300. Ansell Healthcare Products, LLC has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 19, 2013
- Date Received
- August 14, 2012
- 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.