Medical Device Recalls
-
1 to 7 of 7 Results
510(K) Number: K021168 |
|
Results per Page |
Product Description
|
Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
|
---|---|---|---|
Welch Allyn AED 10 automatic external defibrillator and MRL Jumpstart (collectively "AED 10") | 2 | 07/06/2009 | Welch Allyn Protocol, Inc |
Welch Allyn AED 10 automated external defibrillator and MRL Jumpstart (collectively "AED 10") | 2 | 06/23/2009 | Welch Allyn Protocol, Inc |
Welch Allyn AED 10 automated external defibrillator and MRL Jumpstart (collectively "AED 10") | 1 | 03/10/2009 | Welch Allyn Protocol, Inc |
Welch Allyn AED 10 Automated External Defibrillator | 1 | 03/10/2009 | Welch Allyn Protocol, Inc |
Welch Allyn AED 10 automated external defibrillator and MRL Jumpstart (collectively "AED 10") | 1 | 03/09/2009 | Welch Allyn Protocol, Inc |
Welch Allyn AED 10, Automated External Defibrillator, a portable 12V internal battery powered defibr... | 1 | 11/06/2007 | Welch Allyn Protocol, Inc |
Welch Allyn AED 10 Defibrillator; a battery powered automated external defibrillator; Manufacturer: ... | 2 | 07/20/2004 | MRL, Inc., A Welch Allyn Company |
-