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 |