The following data is part of a premarket notification filed by Femcap Incorporated with the FDA for Femmycycle.
| Device ID | K121857 |
| 510k Number | K121857 |
| Device Name: | FEMMYCYCLE |
| Classification | Cup, Menstrual |
| Applicant | FEMCAP INCORPORATED 27001 LA PAZ ROAD, SUITE 312 Mission Viejo, CA 92691 |
| Contact | Albert Rego |
| Correspondent | Albert Rego FEMCAP INCORPORATED 27001 LA PAZ ROAD, SUITE 312 Mission Viejo, CA 92691 |
| Product Code | HHE |
| CFR Regulation Number | 884.5400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-06-26 |
| Decision Date | 2012-11-15 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FEMMYCYCLE 90582413 not registered Live/Pending |
Excellus Holdings, LLC 2021-03-16 |
![]() FEMMYCYCLE 85521562 4325449 Live/Registered |
EXCELLUS HOLDINGS LLC 2012-01-20 |