Viratek, Inc.
FDA Regulatory Profile
Viratek, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 9, 1990.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K896608 | SPAG PAK | April 9, 1990 |
| K882396 | AEROSOL DELIVERY HOOD | August 1, 1988 |
| K870051 | SPAG-2 AEROSOL GENERATOR W/USE OF VIRAZOLE | October 6, 1987 |
| K871427 | (SPAG) MODEL SPAG-2 6000 SERIES | October 6, 1987 |
| K843717 | VIRATEK SMALL PARTICLE AEROSOL GENERAT | December 30, 1985 |