FDA 510(k) Applications Submitted by Judith Blunt

FDA 510(k) Number Submission Date Device Name Applicant
K980839 03/04/1998 AVOCET PT AVOCET MEDICAL, INC.
K020679 03/04/2002 INRATIO HEMOSENSE, INC.
K980982 03/17/1998 AVOCET SYSTEM LIQUID CONTROL LEVEL 1 AND LEVEL 2 AVOCET MEDICAL, INC.
K991286 04/15/1999 AVOCET ACUSURE SYSTEM AVOCET MEDICAL, INC.
K021923 06/11/2002 INRATIO SELF-TEST HEMOSENSE, INC.


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