Sechrist Industries, Inc. - FDA 510(k) Cleared Devices
23
Total
22
Cleared
0
Denied
Sechrist Industries, Inc. has 22 FDA 510(k) cleared anesthesiology devices. Based in Mchenry, US.
Historical record: 22 cleared submissions from 1978 to 2014.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
23 devices
Cleared
May 30, 2014
SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER
Anesthesiology
86d
Cleared
Apr 26, 2010
SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER
Anesthesiology
87d
Cleared
Oct 28, 2005
MODEL 3300E/ER MONOPLACE HYPERBARIC OXYGEN CHAMBER
Anesthesiology
29d
Cleared
Jan 17, 2003
SECHRIST AIR/OXYGEN MIXER, MODEL 3500 CP-G
Cardiovascular
71d
Cleared
Nov 10, 1999
MILLENNIUM INFANT VENTILATOR
Anesthesiology
49d
Cleared
Aug 10, 1999
SECHRIST AIR-OXYGEN MIXER, 3500/3500HL SERIES
Anesthesiology
14d
Cleared
Jun 13, 1995
MODEL 2500E/2500ER HYPERBARIC CHAMBER
Anesthesiology
655d
Cleared
Jun 13, 1995
MODEL 3200P/3200PR HYPERBARIC CHAMBER
Anesthesiology
132d
Cleared
Sep 16, 1993
THE INFANT FLOW SYSTEM
Anesthesiology
217d
Cleared
Nov 02, 1992
SEHRIST VOLUME VENTILATOR, MODEL 2200B
Anesthesiology
382d
Cleared
May 18, 1990
SECHRIST VOLUME VENTILATOR MODEL 2200B
Anesthesiology
199d
Cleared
Dec 22, 1989
SECHRIST DISPOSABLE INFANT BREATHING CIRCUIT
Anesthesiology
80d