FDA 510(k) Applications Submitted by B. J COLLEYPRIEST

FDA 510(k) Number Submission Date Device Name Applicant
K001677 06/01/2000 BABY DOPPLEX 4000 (BD4000) HUNTLEIGH DIAGNOSTICS LTD.
K010889 03/26/2001 BABY DOPPLEX 3000 MK 2 (BD3000) HUNTLEIGH HEALTHCARE, INC.
K010894 03/26/2001 BABY DOPPLEX 3002 (BD3002) HUNTLEIGH HEALTHCARE, INC.
K032315 07/28/2003 IOP8 INTRA OPERATIVE PROBE HUNTLEIGH HEALTHCARE, INC.
K002548 08/17/2000 FETAL ASSIST HUNTLEIGH DIAGNOSTICS LTD.


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