FDA 510(k) Applications Submitted by ROBERT H SCHIFFMAN, R.A.C.
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. |
|
|