Laborie Medical Tech Corp.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K993721 | UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES | KPI | 1999-11-29 | View |
| 510(k) | K990041 | UROSTYM BIOFEEDBACK AND STIMULATION PROBES | KPI | 1999-08-05 | View |
| 510(k) | K991479 | VISER PENILE TUMESCENCE MONITOR | LIL | 1999-07-07 | View |
| 510(k) | K963064 | ANO-RECTAL MANOMETRY OPTION, MODEL NUMBER UDS-ARM | FFX | 1997-06-05 | View |
| 510(k) | K950016 | CART, MODE NUMBER UDS-CART | FEN | 1995-03-30 | View |
No matching devices.
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