Laborie Medical Tech Corp.
Laborie Medical Tech Corp. appears in FDA public data with 0 recalls, 6 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on Nov 29, 1999.
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 | Nov 29, 1999 |
| K990041 | UROSTYM BIOFEEDBACK AND STIMULATION PROBES | Aug 5, 1999 |
| K991479 | VISER PENILE TUMESCENCE MONITOR | Jul 7, 1999 |
| K963064 | ANO-RECTAL MANOMETRY OPTION, MODEL NUMBER UDS-ARM | Jun 5, 1997 |
| K950016 | CART, MODE NUMBER UDS-CART | Mar 30, 1995 |
| K941105 | UORCAP,MODEL NUMBER UDS-UCAP | May 10, 1994 |