Atlas FDA

MRL, Inc., A Welch Allyn Company

5 FDA 510(k) clearances · Recalling firm

Sort:Newest firstOldest first

◉ Watch MRL, Inc., A Welch Allyn Company

RecordFirmDate
Welch Allyn PIC 50 Portable Intensive Care System, Multi-Parameter Monitor/Defibrillator; recall (Z-0343-2007)MRL, Inc., A Welch Allyn Company2007-01-19
Welch Allyn PIC 50 Portable Intensive Care System Multi-Parameter Monitor/Defibrillator; a recall (Z-1195-06)MRL, Inc., A Welch Allyn Company2006-07-08
Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powe recall (Z-1106-06)MRL, Inc., A Welch Allyn Company2006-06-22
Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powe recall (Z-0806-05)MRL, Inc., A Welch Allyn Company2005-05-12
Welch Allyn AED 10 Defibrillator; a battery powered automated external defibrillator; Manu recall (Z-0918-04)MRL, Inc., A Welch Allyn Company2004-07-20

Track MRL, Inc., A Welch Allyn Company automatically

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