FDA 510(k) Applications for Medical Device Product Code "JEQ"
|
FDA 510(k) Number | Applicant | Device Name | Decision Date |
K061199 | BRAUN GMBH | ORAL B PROFESSIONALCARE SERIES, ORAL B ADVANCEPOWER SERIES | 05/31/2006 |
K061351 | BRAUN GMBH | ORAL-B SONIC COMPLETE | 06/05/2006 |
K970381 | EMJOI ACTION USA, LTD. | POWERED TOOTHBRUSH | 04/18/1997 |
K012914 | HOMEDICS, INC. | SONICWAVE SONIC PLAQUE REMOVER | 10/01/2001 |
K022900 | JOHN O. BUTLER CO. | BUTLER GUM VARI-CLEAN POWER TOOTHBRUSHES | 11/14/2002 |
K040416 | PHILIPS ORAL HEALTHCARE, INC. | SONICARE ADVANCE TOOTHBRUSH, MODEL 4900 | 07/02/2004 |
K141018 | PROCTER & GAMBLE CO. | ORAL-B TEST DRIVE POWER BRUSH TRIAL PROGRAM KIT, ORAL-B TEST DRIVE POWER TOOTHBRUSH KIT, ORAL-B TEST DRIVE REFILL KIT | 09/15/2014 |
K200881 | The Procter & Gamble Company | Oral-B iO Test Drive Power Brush Trial Program Kit | 08/27/2020 |