510(k) K150883
K150883 is an FDA 510(k) premarket notification submitted by Fidia Farmaceutici S.P.A. for the device "HyaloGYN Vaginal Hydrating Gel". The FDA issued a decision of Substantially Equivalent on Sep 1, 2015. The device falls under product code NUC (Lubricant, Personal), a Class II device regulated under 21 CFR 884.5300. Fidia Farmaceutici S.P.A. has 2 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Sep 1, 2015
- Date Received
- Apr 2, 2015
- 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
- 510(k)
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.