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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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