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FDA 510(k) Applications Submitted by CASCO-NERL DIAGNOSTICS CORPORATION (MAINE)
FDA 510(k) Number
Submission Date
Device Name
Applicant
K992034
06/16/1999
DOCUMENT THYROID CAL*VER
CASCO-NERL DIAGNOSTICS CORPORATION (MAINE)
K002174
07/19/2000
DOCUMENT ASSAYED CHEMISTRY CONTROL, LEVELS 1, 2 AND3
CASCO-NERL DIAGNOSTICS CORPORATION (MAINE)
K993014
09/08/1999
MODIFICATION TO DOCUMENT THYROID CAL.VER
CASCO-NERL DIAGNOSTICS CORPORATION (MAINE)
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