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 |