The following data is part of a premarket notification filed by Samsung Medison Co., Ltd with the FDA for Rs85 Diagnostic Ultrasound System.
Device ID | K191115 |
510k Number | K191115 |
Device Name: | RS85 Diagnostic Ultrasound System |
Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
Applicant | Samsung Medison Co., Ltd 3366 Hanseo-ro,Nam-myeon Hongcheon-gun, KR 25108 |
Contact | Ji Yea Lee |
Correspondent | Ji Yea Lee Samsung Medison Co., Ltd 3366, Hanseo-ro, Nam-myeon Hongcheon-gun, Gangwon-do, KR 25108 |
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 | 2019-04-26 |
Decision Date | 2019-06-12 |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08809521023831 | K191115 | 000 |