FDA 510(k) Applications Submitted by ROBERT SCHIFFMAN

FDA 510(k) Number Submission Date Device Name Applicant
K100020 01/05/2010 DX SERIES FINGER SENSOR DIXTAL MEDICAL INC.
K000794 03/13/2000 MODIFICATION TO MARSPO2, MODEL 2001 NOVAMETRIX MEDICAL SYSTEMS, INC.
K982499 07/20/1998 COSMO PLUS WITH NICO, MODEL 8200 NOVAMETRIX MEDICAL SYSTEMS, INC.
K963327 08/23/1996 TIDAL WAVE CARBON DIOXIDE MONITOR, MODEL 610 NOVAMETRIX MEDICAL SYSTEMS, INC.
K963380 08/27/1996 CO 2 SMO PLUS NOVAMETRIX MEDICAL SYSTEMS, INC.
K103285 11/08/2010 DIXTAL DZ-4100 SERIES PULSE OXIMETER DIXTAL MEDICAL, INC.
K993979 11/24/1999 MARSPO2, MODEL 2001 NOVAMETRIX MEDICAL SYSTEMS, INC.
K010451 02/15/2001 NOVAMETRIX MARQUETTE COMPATIBLE SENSORS NOVAMETRIX MEDICAL SYSTEMS, INC.
K960831 02/29/1996 VENTRAK RMMS 1550 NOVAMETRIX MEDICAL SYSTEMS, INC.
K964360 11/01/1996 VENT(VENTCHECK) HANDHELD RESPIRATORY/MECHANICS MONITOR MODEL 101 NOVAMETRIX MEDICAL SYSTEMS, INC.


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