Medical Device Recalls
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1 to 3 of 3 Results
510(K) Number: K002232 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibr... | 1 | 09/19/2007 | Welch Allyn Protocol, Inc |
Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibr... | 1 | 06/22/2006 | MRL, Inc., A Welch Allyn Company |
Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibr... | 1 | 05/12/2005 | MRL, Inc., A Welch Allyn Company |
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