The following data is part of a premarket notification filed by Samsung Medison Co., Ltd with the FDA for Ugeo Pt60a Diagnostic Ultrasound System.
Device ID | K132228 |
510k Number | K132228 |
Device Name: | UGEO PT60A DIAGNOSTIC ULTRASOUND SYSTEM |
Classification | System, Imaging, Pulsed Echo, Ultrasonic |
Applicant | SAMSUNG MEDISON CO., LTD 42, TEHERAN-RO 108-GIL GANGNAM-GU Seoul, KR |
Contact | Kyeong-mi Park |
Product Code | IYO |
Subsequent Product Code | ITX |
Subsequent Product Code | IYN |
CFR Regulation Number | 892.1560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | Yes |
Combination Product | No |
Date Received | 2013-07-17 |
Decision Date | 2013-08-20 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
08806167745271 | K132228 | 000 |