The following data is part of a premarket notification filed by Ob The-addition, Llc with the FDA for The Addition.
| Device ID | K102683 |
| 510k Number | K102683 |
| Device Name: | THE ADDITION |
| Classification | Media, Coupling, Ultrasound |
| Applicant | OB THE-ADDITION, LLC 2206 MODOC ROAD #3 Santa Barbara, CA 93101 |
| Contact | Rebecca K Pine |
| Correspondent | Rebecca K Pine OB THE-ADDITION, LLC 2206 MODOC ROAD #3 Santa Barbara, CA 93101 |
| Product Code | MUI |
| CFR Regulation Number | 892.1570 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2010-09-17 |
| Decision Date | 2011-01-06 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() THE ADDITION 86368636 4722918 Live/Registered |
Flewellen, Bradford 2014-08-16 |
![]() THE ADDITION 78510213 3035428 Dead/Cancelled |
NM NEVADA TRUST 2004-11-02 |