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 |