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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