The following data is part of a premarket notification filed by Librette, Inc with the FDA for Bellecup.
| Device ID | K092985 |
| 510k Number | K092985 |
| Device Name: | BELLECUP |
| Classification | Cup, Menstrual |
| Applicant | LIBRETTE, INC 1705. S. CAPITAL OF TEXAS HWY SUITE 500 Austin, TX 78746 |
| Contact | Neal Kolber |
| Correspondent | Neal Kolber LIBRETTE, INC 1705. S. CAPITAL OF TEXAS HWY SUITE 500 Austin, TX 78746 |
| Product Code | HHE |
| CFR Regulation Number | 884.5400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-28 |
| Decision Date | 2010-06-28 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BELLECUP 85126211 not registered Dead/Abandoned |
Veilso, Corp. 2010-09-09 |