FDA 510(k) Applications Submitted by RIEKO SO
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K024373 | 12/31/2002 | MODIFICATION TO ANIMEC, MODELS AM-2S-4, AM-2S-5, LT-1-4 & LT-1-5 | ELLTEC CO., LTD. |
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