The following data is part of a premarket notification filed by Medison Co., Ltd. with the FDA for Accuvix V20 Diagnostic Ultrasound System.
| Device ID | K092159 |
| 510k Number | K092159 |
| Device Name: | ACCUVIX V20 DIAGNOSTIC ULTRASOUND SYSTEM |
| Classification | System, Imaging, Pulsed Doppler, Ultrasonic |
| Applicant | MEDISON CO., LTD. 1003, DAECHI-DONG GANGNAM-GU Seoul, KR 135-280 |
| Contact | Shim Kyung-am |
| Correspondent | Mark Job REGULATORY TECHNOLOGY SERVICES, LLC 1000 Westgate Drive, Suite 510k Saint Paul, MN 55114 |
| Product Code | IYN |
| CFR Regulation Number | 892.1550 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | Yes |
| Combination Product | No |
| Date Received | 2009-07-16 |
| Decision Date | 2009-07-28 |
| Summary: | summary |