510(k) K002232 ยท MKJ Automated External Defibrillators (Non-Wearable)
AEDEFIBRILLATOR
| Applicant | Medical Research Laboratories, Inc., Buffalo Grove IL, US |
| Decision | Substantially Equivalent, Dec 6, 2000 |
| Received | Jul 24, 2000 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K002232
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 19, 2007 | Welch Allyn Protocol, Inc Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibrillator; Manufactured by MRL Inc., A Welch Allyn Company, Buffalo Grove, Illinois; Model AED 20, Cat Terminated |
MKJ | None listed |
| Jun 22, 2006 | MRL, Inc., A Welch Allyn Company Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibrillator; Manufactured by MRL Inc., A Welch Allyn Company, 1000 Asbury Drive, Buffalo Grove, Illinois Terminated |
MKJ | None listed |
| May 12, 2005 | MRL, Inc., A Welch Allyn Company Welch Allyn AED 20 Automated External Defibrillator; a portable, 12V internal battery powered defibrillator; Manufactured by MRL Inc., A Welch Allyn Company, 1000 Asbury Drive, Buffalo Grove, Illinois Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.