The following data is part of a premarket notification filed by Bk Medical Aps with the FDA for Bk2300.
| Device ID | K161960 |
| 510k Number | K161960 |
| Device Name: | Bk2300 |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | BK MEDICAL APS MILEPARKEN 34 Herlev, DK 2730 |
| Contact | Michael J. Doyle |
| Correspondent | Karen Provencher BK MEDICAL APS MILEPARKEN 34 Herlev, DK 2730 |
| Product Code | IYN |
| Subsequent Product Code | ITX |
| Subsequent Product Code | IYO |
| CFR Regulation Number | 892.1550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-07-18 |
| Decision Date | 2016-10-17 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 05704916000899 | K161960 | 000 |