The following data is part of a premarket notification filed by Shimadzu Corp. with the FDA for Sdu-500 Diagnostic Ultrasound Instrument.
| Device ID | K875187 |
| 510k Number | K875187 |
| Device Name: | SDU-500 DIAGNOSTIC ULTRASOUND INSTRUMENT |
| Classification | System, Imaging, Pulsed Echo, Ultrasonic |
| Applicant | SHIMADZU CORP. 1 NISHINOKYO-KUWABARACHO NAKAYGO-KU Kyoto City 604 Japan, JP |
| Contact | Takao Someyama |
| Correspondent | Takao Someyama SHIMADZU CORP. 1 NISHINOKYO-KUWABARACHO NAKAYGO-KU Kyoto City 604 Japan, JP |
| Product Code | IYO |
| CFR Regulation Number | 892.1560 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-12-22 |
| Decision Date | 1988-12-12 |