510(k) K014209 ยท MKJ Automated External Defibrillators (Non-Wearable)
PADPRO MODEL 2001, 2001-S, 2001-C, 2001-EPS
| Applicant | Padpro, LLC, Deer Field IL, US |
| Decision | Substantially Equivalent, Jan 18, 2002 |
| Received | Dec 21, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K014209
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 4, 2014 | ConMed Corporation ADULT Radiotransparent Electrode, REF/Catalog Number 2001H, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR
Intended for use during defibrillation, cardioversion, Terminated |
MKJ | None listed |
| Dec 4, 2014 | ConMed Corporation ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-C, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR Terminated |
MKJ | None listed |
| Dec 4, 2014 | ConMed Corporation ADULT Radiotransparent Electrode, REF/Catalog Number 2001H-PC, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR Terminated |
MKJ | None listed |
| May 13, 2013 | ConMed Corporation PadPro(R) Adult Radiotransparent Multifunction Electrodes, REF/Catalog No. 2001M-C.
The PadPro(R) Adult Radiotransparent Multifunction Electrodes with Carbon Leadwires and Medtronic(R) Connector are Terminated |
MKJ | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.