K190872 is an FDA 510(k) clearance for the BioGenesis Fertility Lubricant, a Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible (Class II — Special Controls, product code PEB), submitted by Good Clean Love, Inc. (Eugene, US). The FDA issued a Cleared decision on November 7, 2019, 218 days after receiving the submission on April 3, 2019. This device falls under the Obstetrics & Gynecology review panel. Regulated under 21 CFR 884.5300.
| 510(k) Number | K190872 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | April 03, 2019 |
| Decision Date | November 07, 2019 |
| Days to Decision | 218 days |
| Submission Type | Traditional |
| Review Panel | Obstetrics & Gynecology (OB) |
| Summary | Summary PDF |
| Product Code | PEB — Lubricant, Personal, Gamete, Fertilization, And Embryo Compatible |
| Device Class | Class II — Special Controls |
| CFR Regulation | 21 CFR 884.5300 |
| Definition | 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. |