510(k) K101241
K101241 is an FDA 510(k) premarket notification submitted by Lil Drug Store Products, Inc. for the device "REPLENS LONG-LASTING VAGINAL MOISTURIZER (PRE-FILLED APPLICATOR)". The FDA issued a decision of Substantially Equivalent on August 17, 2010. The device falls under product code NUC (Lubricant, Personal), a Class II device regulated under 21 CFR 884.5300. Lil Drug Store Products, Inc. has at least 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 17, 2010
- Date Received
- May 4, 2010
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- Yes
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.