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FDA 510(k) Applications Submitted by GRADIPORE LTD.
FDA 510(k) Number
Submission Date
Device Name
Applicant
K992456
07/23/1999
GRADILEIDEN V TEST
GRADIPORE LTD.
K993332
10/04/1999
GRADIPLASMA LA HIGH, GRADIPLASMA LA LOW MODELS LAHP-1, LAHP-05, LALP-1, LALP-05
GRADIPORE LTD.
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