Company ยท CA
Diros Technology, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 2002 to 2017. Name variants (Inc, Corp, punctuation) are merged.
8510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Jun 27, 2017 | K170708 | OWL RF INSULATED CANNULAE Diros Technology, Inc., CA | GXI |
| Jul 30, 2015 | K150371 | Diros OWL Sterile Single Use TridentTM R.F. Insulated Cannulae,Models DTR and DTRH Diros Technology, Inc., CA | GXI |
| Dec 30, 2014 | K141586 | OWL CANNULAE Diros Technology, Inc., CA | GXI |
| Jun 3, 2011 | K102566 | OWL CANNULAE Diros Technology, Inc., CA | GXI |
| May 5, 2011 | K110593 | OWL RF PROBES Diros Technology, Inc., CA | GXI |
| Jan 22, 2010 | K093185 | OWL UNIVERSAL RF SYSTEM URF-3AP (ML) Diros Technology, Inc., CA | GXD |
| Sep 27, 2006 | K062758 | OWL URF-3AP Diros Technology, Inc., CA | GXD |
| Jul 1, 2002 | K021869 | OWL RADIOFREQUENCY SYSTEM, MODEL URF-2AP Diros Technology, Inc. | GXD |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||