Laborie Medical Tech Corp.
FDA Regulatory Profile
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 6
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K993721 | UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES | November 29, 1999 |
| K990041 | UROSTYM BIOFEEDBACK AND STIMULATION PROBES | August 5, 1999 |
| K991479 | VISER PENILE TUMESCENCE MONITOR | July 7, 1999 |
| K963064 | ANO-RECTAL MANOMETRY OPTION, MODEL NUMBER UDS-ARM | June 5, 1997 |
| K950016 | CART, MODE NUMBER UDS-CART | March 30, 1995 |
| K941105 | UORCAP,MODEL NUMBER UDS-UCAP | May 10, 1994 |