The following data is part of a premarket notification filed by Bk Medical Aps with the FDA for Ultrasound Scanner System Bk2300.
| Device ID | K151910 |
| 510k Number | K151910 |
| Device Name: | Ultrasound Scanner System BK2300 |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | BK MEDICAL APS MILEPARKEN 34 Herlev, DK Dk-2730 |
| Contact | Randi Hauerberg |
| Correspondent | Randi Hauerberg BK MEDICAL APS MILEPARKEN 34 Herlev, DK Dk-2730 |
| Product Code | IYN |
| Subsequent Product Code | ITX |
| Subsequent Product Code | IYO |
| CFR Regulation Number | 892.1550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-07-13 |
| Decision Date | 2015-10-05 |
| Summary: | summary |