510(k) K020203 ยท MKJ Automated External Defibrillators (Non-Wearable)
PADPRO MODEL #2516
| Applicant | Padpro, LLC, Deer Field IL, US |
| Decision | Substantially Equivalent, May 8, 2002 |
| Received | Jan 22, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K020203
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Dec 4, 2014 | ConMed Corporation ADULT Radiotransparent Electrode, REF/Catalog Number 2516H, 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 2516H-PC, Rx ONLY --- COMPARABLE TO PHILIPS MEDICAL HEARTSTART ELECTRODES PLUG STYLE CONNECTOR Terminated |
MKJ | None listed |
| Apr 24, 2007 | Conmed Corporation PADPRO ADULT Radiotranslucent Pad w/Zoll connector. Defibrillation/Pacing/Cardioversion/Monitoring Electrodes, REF/Catalog # 2516Z. RX ONLY. Made in USA for: CONMED CORPORATION Utica, New York, 13502. Terminated |
MLN | None listed |
| Apr 24, 2007 | Conmed Corporation PADPRO ADULT Radiotranslucent Pad w/Medtronic connector, REF/Catalog #2516M. RX ONLY. Defibrillation/Pacing/Cardioversion/Monitoring Electrodes. Made in USA for: CONMED CORPORATION Utica, New York, 13 Terminated |
MLN | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.