Hudson Respiratory Care, Inc. - FDA 510(k) Cleared Devices
15
Total
15
Cleared
0
Denied
Hudson Respiratory Care, Inc. has 15 FDA 510(k) cleared anesthesiology devices. Based in Temecula, US.
Historical record: 15 cleared submissions from 1990 to 2003.
Browse the complete list of FDA 510(k) cleared anesthesiology devices from this manufacturer. Filter by specialty or product code using the sidebar.
15 devices
Cleared
Jul 07, 2003
MODEL 780
Anesthesiology
67d
Cleared
Jun 13, 2001
NASAL CANNULA, WITH AND WITHOUT SUPPLY TUBING, AND OTHER SIMILAR NASAL...
Anesthesiology
61d
Cleared
Jun 13, 2001
OXYGEN SUPPLY TUBING, MODEL 1115
Anesthesiology
61d
Cleared
Mar 14, 2001
SMOOTH-FLO CIRCUIT
Anesthesiology
30d
Cleared
Nov 03, 2000
CONCHATHERM 2000 HUMIDIFICATION SYSTEM, MODELS 500-00, -10, -20, -30, -40,...
Anesthesiology
203d
Cleared
May 24, 2000
HUDSON RCI CONCHA COLUMN, CAT. NO. 385-40 AND HUDSON RCI CIRCUIT, CAT. NO....
Anesthesiology
231d
Cleared
Mar 22, 2000
SIDE DRAFT NEB-U-MIST NEBULIZER, MODEL 41896
Anesthesiology
90d
Cleared
Feb 21, 1997
HUDSON RCI LIFESAVER SINGLE PATIENT USE MANUAL RESUSCITATOR
Anesthesiology
88d
Cleared
Sep 10, 1996
DUAL LUMEN OXYGEN DELIVERY GAS SAMPLING CANNULA
Anesthesiology
172d
Cleared
Aug 14, 1996
BACTERIA/VIRAL FILTER
General Hospital
89d
Cleared
Mar 12, 1996
CATH-GUIDE
Anesthesiology
91d
Cleared
Dec 21, 1994
HUDSON RCI LIFESAVER SINGLE PATIENT USE MANUAL RESUSCITATOR CATALOG NUMBERS:...
Anesthesiology
106d