The following data is part of a premarket notification filed by Epilady 2000, L.l.c. with the FDA for Robi Combi.
Device ID | K930859 |
510k Number | K930859 |
Device Name: | ROBI COMBI |
Classification | Detectors And Removers, Lice, (including Combs) |
Applicant | EPILADY 2000, L.L.C. 1333 NEW HAMPSHIRE AVE.,N.W. SUITE 400 Washington, DC 20036 |
Contact | Donald E Segal |
Correspondent | Donald E Segal EPILADY 2000, L.L.C. 1333 NEW HAMPSHIRE AVE.,N.W. SUITE 400 Washington, DC 20036 |
Product Code | LJL |
CFR Regulation Number | 880.5960 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-02-18 |
Decision Date | 1994-02-28 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ROBI COMBI 74202284 not registered Dead/Abandoned |
MEPRO EPILADY LTD. 1991-09-10 |