510(k) K093905 ยท CBK Ventilator, Continuous, Facility Use
TRILOGY 202 VENTILATOR
| Applicant | Respironics, Inc., Murrysville PA, US |
| Decision | Substantially Equivalent, May 12, 2010 |
| Received | Dec 22, 2009 |
| Type | Abbreviated |
| FDA record | Open on fda.gov |
Recalls that name K093905
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 7, 2016 | Philips Respironics Trilogy 100, Trilogy 200, Trilogy O2, Trilogy 202,
Trilogy EC, Garbin, Garbin Plus
Trilogy 100, Trilogy 200, Garbin, Garbin plus provides continuous or intermittent ventilatory support for the care o Terminated |
CBK | None listed |
| Mar 6, 2014 | Phillips Respironics, Inc. Trilogy Ventilators
The Respironics Trilogy 100 system provides continuous or intermittent ventilator support for the care of individuals who require mechanical ventilation. Trilogy 100 is intended fo Terminated |
CBK | None listed |
| Jul 23, 2012 | Respironics, Inc. Respironics Trilogy 100, 200, and 202 Ventilators
The Respironics Trilogy systems provides continuous or intermittent ventilatory support for the care of individuals who require mechanical ventilatio Terminated |
CBK | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.