510(k) K012344 ยท NLF Oximeter, Reprocessed
VANGUARD REPROCESSED PULSE OXIMETER SENSORS
| Applicant | Vanguard Medical Concepts, Inc., Lakeland FL, US |
| Decision | Substantially Equivalent, Oct 4, 2002 |
| Received | Jul 24, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K012344
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Sep 19, 2008 | Ascent Healthcare Solutions, Inc. Neonatal/Adult 02 Transducer, (Nellcor), Latex Free. - Reprocessed Sterile device -- Pulse Oximeter. Terminated |
NLF | None listed |
| Sep 19, 2008 | Ascent Healthcare Solutions, Inc. Adult 02 Transducer (Nellcor) - Reprocessed Sterile device -- Pulse Oximeter. Terminated |
NLF | None listed |
| Sep 19, 2008 | Ascent Healthcare Solutions, Inc. Infant 02 Transducer (Nellcor) - Reprocessed Sterile device -- Pulse Oximeter. Terminated |
NLF | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.