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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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