Company ยท US
Laborie Medical Tech Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1994 to 1999. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Nov 29, 1999 | K993721 | UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES Laborie Medical Tech Corp. | KPI |
| Aug 5, 1999 | K990041 | UROSTYM BIOFEEDBACK AND STIMULATION PROBES Laborie Medical Tech Corp. | KPI |
| Jul 7, 1999 | K991479 | VISER PENILE TUMESCENCE MONITOR Laborie Medical Tech Corp. | LIL |
| Jun 5, 1997 | K963064 | ANO-RECTAL MANOMETRY OPTION, MODEL NUMBER UDS-ARM Laborie Medical Tech Corp. | FFX |
| Mar 30, 1995 | K950016 | CART, MODE NUMBER UDS-CART Laborie Medical Tech Corp., CA | FEN |
| May 10, 1994 | K941105 | UORCAP,MODEL NUMBER UDS-UCAP Laborie Medical Tech, Inc., CA | EXY |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||