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Gradipore , Ltd.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K993332
GRADIPLASMA LA HIGH, GRADIPLASMA LA LOW MODELS LAHP-1, LAHP-05, LALP-1, LALP-05
February 16, 2000
K992456
GRADILEIDEN V TEST
December 21, 1999
K922156
LUCOR CONFIRMATORY REAGENT
April 6, 1993
K903037
LUPO-TEST REAGENT
December 17, 1990