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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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