Howtek, Inc.
FDA Regulatory Profile
Howtek, 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 August 12, 2002.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K021949 | FULCRUM | August 12, 2002 |
| K973081 | DIGITIZER DIRECTOR: IMAGE COMPRESSION MODULE (HO4059-REV 2.0) | November 5, 1997 |
| K972191 | DIGITIZER DIRECTOR (HSC025-01) | September 8, 1997 |
| K970908 | HOWTEK 960 | May 20, 1997 |
| K953117 | SCANMASTER DX | January 18, 1996 |