FDA 510(k) Applications Submitted by LORI GLASTETTER

FDA 510(k) Number Submission Date Device Name Applicant
K011702 06/01/2001 VERTIS PNT CONTROL UNIT, VERTIS PNT SAFEGUIDE KIDS, MODELS CU100, SGXXX VERTIS NEUROSCIENCE, INC.
K022241 07/11/2002 VERTIS PNT CONTROL UNIT, MODEL CU 100; VERTIS PNT SAFEGUIDE-CERVICAL, MODEL SG 102-XXX VERTIS NEUROSCIENCE, INC.
K955628 12/11/1995 FORE RUNNER EXTERNAL DEFIBRILLATOR/DEFIBRILLATOR PADS HEARTSTREAM, INC.


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