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 |