Pie Medical Equipment B.V.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 8
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K982203 | CAAS II LVA BIPLANE OPTION | July 14, 1998 |
| K945540 | CAAS II | June 28, 1995 |
| K915647 | DIAGNOSTIC ULTRASOUND SYSTEM MODEL SC250 | November 9, 1992 |
| K912819 | SC1150 CW/PD | January 9, 1992 |
| K911584 | DIAGNOSTIC ULTRASOUND SYSTEM MODEL SC480 | October 24, 1991 |
| K911043 | HEMISPHERE MULTIPLANE ENDORECTAL PROBE | October 9, 1991 |
| K911044 | 7.5 MHZ APAS TRANSDUCER (ART.NOL: 50.04918.1) | October 7, 1991 |
| K900838 | TRANSVAGINAL TRANSDUCER ASSEMBLY | May 23, 1990 |