The following data is part of a premarket notification filed by Bk Medical Aps with the FDA for Ultrasound Scanner System Bk2300.
Device ID | K152052 |
510k Number | K152052 |
Device Name: | Ultrasound Scanner System Bk2300 |
Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant | BK MEDICAL APS MILEPARKEN 34 Herlev, DK Dk-2730 |
Contact | Michael J. Doyle |
Correspondent | Michael J. Doyle 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 | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-07-23 |
Decision Date | 2015-09-16 |
Summary: | summary |