The following data is part of a premarket notification filed by Bk Medical Aps with the FDA for Ultrasound Scanner System Bk2300.
Device ID | K143298 |
510k Number | K143298 |
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 | 2014-11-17 |
Decision Date | 2015-01-16 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
05704916000158 | K143298 | 000 |