FDA 510(k) Applications Submitted by GERALD MCMORROW

FDA 510(k) Number Submission Date Device Name Applicant
K982568 07/23/1998 BLADDERMANAGER PCI 5000 MODEL 1002 DIAGNOSTIC ULTRASOUND CORP.
K955840 12/26/1995 BLADDERMANAGER PCI 5000 / BLADDERSCAN BVI 5000 DIAGNOSTIC ULTRASOUND CORP.
K955942 12/26/1995 BLADDERSCAN BVI 5000 DIAGNOSTIC ULTRASOUND CORP.
K963585 09/09/1996 BLADDER MANAGER PCI 5000, BLADDERSCAN BVI 5000 DIAGNOSTIC ULTRASOUND CORP.


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