Atlas FDA

Del Mar Reynolds Medical, Ltd.

10 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch Del Mar Reynolds Medical, Ltd.

RecordFirmDate
Spacelabs Pediatric Flow Sensor Kit, PN: 376-0561-00. This kit is for Spacelabs Healthcare recall (Z-1458-2015)Del Mar Reynolds Medical, Ltd.2015-04-20
SpaceLabs Arkon Anesthesia Delivery System with Version 2.0 Software installed. This syste recall (Z-1442-2014)Del Mar Reynolds Medical, Ltd.2014-04-12
CAS I/II Absorbers that are parts of the BleaseSirius Anesthesia Workstation, the BleaseFo recall (Z-0352-2014)Del Mar Reynolds Medical, Ltd.2013-11-20
Spacelabs ARKON Anesthesia Workstation. Spacelabs ARKON Anesthesia Workstation may be used recall (Z-1771-2013)Del Mar Reynolds Medical, Ltd.2013-07-19
Spacelabs BleaseSirius Anesthesia Workstation, BleaseFocus Anesthesia Workstation, and CAS recall (Z-0968-2013)Del Mar Reynolds Medical, Ltd.2013-03-20
BleaseFocus Anesthesia Workstation and 700/900 Series Ventilators are anesthesia gas machi recall (Z-0565-2013)Del Mar Reynolds Medical, Ltd.2012-12-19
Affected device is Model 98400-SL6-AHA, CardioExpress Electrocardiograph. The ECG cable pa recall (Z-0743-2012)Del Mar Reynolds Medical, Ltd.2012-01-13
Lifescreen Apnea is Lifescreen ECG Screening System, Version 3.31. Lifescreen Apnea is ind recall (Z-0520-2012)Del Mar Reynolds Medical, Ltd.2012-01-11
Ambulatory Blood Pressure (ABP) Monitor, Model 90217A. The Spacelabs Model 90217A Ambulato recall (Z-0304-2012)Del Mar Reynolds Medical, Ltd.2011-11-29
PDI Electrode Prep Pads, Skin Prep B339 are non-sterile alcohol prep pads. They are includ recall (Z-0262-2012)Del Mar Reynolds Medical, Ltd.2011-11-21

Track Del Mar Reynolds Medical, Ltd. automatically

Every clearance here is in the API, with alerts when new ones post.