Fertility Technology Resources, Inc.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 3
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K041470 | MORTON IUI CATHETERS | November 22, 2004 |
| K032208 | MONA LISA ASPIRATION NEEDLE | December 9, 2003 |
| K023017 | TUCKER EMBRYO CATHETER | December 13, 2002 |
| K992307 | EMBRYO GLIDE EMBRYO TRANSFER CATHETER, EMBRYO GLIDE STYLE FOR EMBRYO TRANSFER CATHETER | September 13, 1999 |