Victus, Inc.
FDA Regulatory Profile
Victus, Inc. appears in FDA public data with 1 recall, 3 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent recall (D-1652-2012, Class II) was initiated on November 10, 2011. Its most recent 510(k) clearance was granted on January 27, 2010.
Summary
- Total Recalls
- 1
- 510(k) Clearances
- 3
- Inspections
- 0
- Compliance Actions
- 0
Recent Recalls
| Number | Class | Product | Date |
|---|
| D-1652-2012 | Class II | Hipoglos Ointment (zinc oxide and lanolin), Helps prevent and treat diaper rash, skin irritation, Ma | November 10, 2011 |
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K093271 | EXTENSION SET (STANDARDBORE TUBING), EXTENSION SET (MINIBORE TUBING), IV ADMINISTRATION SET ( STANDA | January 27, 2010 |
| K030246 | VICTUS I.V. ADMINISTRATION SET, MODELS 27071 AND 27072 | February 26, 2003 |
| K023469 | VICTUS I.V. ADMINISTRATION SET, MODELS 27058, 27059,27062 | December 10, 2002 |