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FDA 510(k) Applications Submitted by B.J. COLLEYPRIEST
FDA 510(k) Number
Submission Date
Device Name
Applicant
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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