The following data is part of a premarket notification filed by Samsung Medison Co., Ltd. with the FDA for Hera W10 Diagnostic Ultrasound System.
| Device ID | K182595 |
| 510k Number | K182595 |
| Device Name: | HERA W10 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, KR 25108 |
| 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 | 2018-09-20 |
| Decision Date | 2018-12-18 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08806167799045 | K182595 | 000 |
| 08806167799038 | K182595 | 000 |
| 08806167799137 | K182595 | 000 |
| 08809521023657 | K182595 | 000 |
| 08809521023626 | K182595 | 000 |
| 08809521023541 | K182595 | 000 |
| 08806167759810 | K182595 | 000 |