Ventrex, Inc.
Ventrex, Inc. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on July 12, 2006.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K061044 | FEATHERLITE AQUA TOCODYNAMOMETER | July 12, 2006 |
| K013477 | TOCO LITE, MODEL TD-01 | January 17, 2002 |
| K964821 | COVEROX SHEATH MODELS NUMBER PS65, PS67, EPS65 AND EPS67 | July 16, 1997 |
| K963415 | VENTREX OXYGEN SENSOR | November 25, 1996 |
| K925044 | VENTREX ALLERGEN DISC | May 14, 1993 |
| K924119 | VENTREX ALLERGEN DISC | November 30, 1992 |