FDA 510(k) Applications Submitted by ELLTEC CO., LTD.

FDA 510(k) Number Submission Date Device Name Applicant
K012906 08/29/2001 ANIMEC, MODELS AM-2S-4 AND AM-2S-5 ELLTEC CO., LTD.
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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