Company ยท US
Ventrex, Inc.
FDA 510(k) clearances and medical device recalls filed under this name, 1992 to 2006. Name variants (Inc, Corp, punctuation) are merged.
6510(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 |
|---|---|---|---|
| Jul 12, 2006 | K061044 | FEATHERLITE AQUA TOCODYNAMOMETER Ventrex, Inc. | HFM |
| Jan 17, 2002 | K013477 | TOCO LITE, MODEL TD-01 Ventrex, Inc. | HFM |
| Jul 16, 1997 | K964821 | COVEROX SHEATH MODELS NUMBER PS65, PS67, EPS65 AND EPS67 Ventrex, Inc. | DQA |
| Nov 25, 1996 | K963415 | VENTREX OXYGEN SENSOR Ventrex, LLC | CCL |
| May 14, 1993 | K925044 | VENTREX ALLERGEN DISC Ventrex, Inc. | DHB |
| Nov 30, 1992 | K924119 | VENTREX ALLERGEN DISC Ventrex, Inc. | DHB |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||