510(k) K051436
K051436 is an FDA 510(k) premarket notification submitted by Ingfertlity, LLC for the device "PRE' VAGINAL LUBRICANT". The FDA issued a decision of Substantially Equivalent on October 13, 2006. The device falls under product code PEB (Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible), a Class II device regulated under 21 CFR 884.5300.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 13, 2006
- Date Received
- June 1, 2005
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible
- Device Class
- Class II
- Regulation Number
- 884.5300
- Review Panel
- OB
- Submission Type
A personal lubricant, for penile and/or vaginal application, intended to moisturize and lubricate, to enhance the ease and comfort of sexual activity and supplement the body's natural lubrication. This device may or may not be compatible with natural rubber latex, polyisoprene, and/or polyurethane condoms. This device is compatible with sperm, oocytes, and embryos and can be used by couples trying to conceive. This device may also be used during fertility interventions to facilitate entry of diagnostic and therapeutic devices.