The following data is part of a premarket notification filed by Alpinion Medical Systems Co., Ltd. with the FDA for X-cube 50, X-cube 60.
| Device ID | K220857 |
| 510k Number | K220857 |
| Device Name: | X-CUBE 50, X-CUBE 60 |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | Alpinion Medical Systems Co., Ltd. 5FL, I Dong, 77, Heungan-daero 81beon-gil Dongan-gu Anyang-si, KR 14117 |
| Contact | Boyeon Cho |
| Correspondent | Boyeon Cho Alpinion Medical Systems Co., Ltd. 5FL, I Dong, 77, Heungan-daero 81beon-gil Dongan-gu Anyang-si, KR 14117 |
| 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 | 2022-03-23 |
| Decision Date | 2022-10-13 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08800013545008 | K220857 | 000 |
| 08800013544001 | K220857 | 000 |