FDA 510(k) Applications Submitted by ALOKA CO. LTD USA
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K041916 | 07/16/2004 | ALOKA SSD-ALPHA 5 ULTRASOUND SYSTEM | ALOKA CO. LTD USA |
| K032875 | 09/15/2003 | ALOKA MODEL SSD-5500 V6.0 ULTRASOUND SYSTEM | ALOKA CO. LTD USA |
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