Protek Medical Products, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 9
- Inspections
- 4
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K973958 | GENERAL PURPOSE ATL NEEDLE GUIDE KIT | January 22, 1998 |
| K973622 | TRANSDUCER POSITIONER | November 26, 1997 |
| K970889 | ULTRASOUND TRANSDUCER DRAPE | October 20, 1997 |
| K970893 | ULTRASOUND TRANSDUCER DRAPE | October 20, 1997 |
| K973362 | NEEDLE GUIDE/GRID | October 1, 1997 |
| K970885 | ULTRASOUND SYSTEMS DRAPE | September 22, 1997 |
| K970891 | DRAPE, SURGICAL-LATEX | August 22, 1997 |
| K971722 | TRANS VAGINAL NEEDLE GUIDE | July 10, 1997 |
| K971115 | GE MEDICAL-NEEDLE GUIDE FOR SV, TR ANDATF, ACUSON-NEEDLE GUIDE | June 13, 1997 |