The following data is part of a premarket notification filed by Ue Lifesciences, Inc. with the FDA for Ibreastexam.
| Device ID | K142926 |
| 510k Number | K142926 |
| Device Name: | IBreastExam |
| Classification | System, Documentation, Breast Lesion |
| Applicant | UE LIFESCIENCES, INC. 3711 MARKET STREET, SUITE 800 Philadelphia, PA 19104 |
| Contact | Mihir Shah |
| Correspondent | Mihir Shah UE LIFESCIENCES, INC. 3711 MARKET STREET, SUITE 800 Philadelphia, PA 19104 |
| Product Code | NKA |
| CFR Regulation Number | 884.2990 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-10-08 |
| Decision Date | 2015-04-23 |
| Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() IBREASTEXAM 97259724 not registered Live/Pending |
UE LIFESCIENCES INC. 2022-02-09 |