The following data is part of a premarket notification filed by Samsung Medison Co., Ltd with the FDA for H60 V2.00 Diagnostic Ultrasound System.
| Device ID | K143264 |
| 510k Number | K143264 |
| Device Name: | H60 V2.00 Diagnostic Ultrasound System |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | SAMSUNG MEDISON CO., LTD 42, TEHERAN-RO 108-GIL GANGNAM-GU Seoul, KR 135-280 |
| Contact | Kyeong-mi Park |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| 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 | Yes |
| Combination Product | No |
| Date Received | 2014-11-13 |
| Decision Date | 2014-12-09 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08806167798048 | K143264 | 000 |