Amedic USA
Amedic USA appears in FDA public data with 0 recalls, 10 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on January 4, 1990.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 10
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K897120 | EQUIP COVERS, STERILE | January 4, 1990 |
| K892070 | GENERAL IVT NEEDLE GUIDE KIT, STERILE | September 5, 1989 |
| K892069 | EXTENDED COVERS, STERILE | August 8, 1989 |
| K892071 | GENERAL (BIOPSY) NEEDLE GUIDE KIT, STERILE | August 8, 1989 |
| K892068 | TRT (ACUSON) NEEDLE GUIDE KIT, STERILE | August 4, 1989 |
| K871467 | BIOPSY NEEDLE GUIDE KIT, STERILE | August 21, 1987 |
| K871609 | ULTRASOUND TRANSDUCER SHEATHS, STERILE | July 15, 1987 |
| K871565 | ULTRASOUND TRANSDUCER GEL, STERILE | July 15, 1987 |
| K871503 | BIOPSY NEEDLE GUIDE KIT, STERILE | July 10, 1987 |
| K864219 | TRANSVAGINAL ULTRASOUND BIOPSY NEEDLE GUIDE | March 27, 1987 |