510(k) K020668 ยท IYO System, Imaging, Pulsed Echo, Ultrasonic
ALOKA SSD-1000 DIAGNOSTIC ULTRASOUND SYSTEM, MODELS ASU-1003, UST-9121, UST-9124
| Applicant | Aloka Co., Ltd., Wallingford CT, US |
| Decision | Substantially Equivalent, Jul 10, 2002 |
| Received | Mar 1, 2002 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K020668
No recall in the FDA data names this 510(k).
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