Laborie Medical Tech Corp. is one of 208 FDA 510(k) medical device manufacturers from Canada in the dataset, ranked by real submission volume.
Laborie Medical Tech Corp. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Laborie Medical Tech Corp. has 5 FDA 510(k) cleared medical devices. Based in Mississauga, CA.
Historical record: 5 cleared submissions from 1995 to 1999. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Laborie Medical Tech Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Laborie Medical Tech Corp.
5 devices
Cleared
Nov 29, 1999
UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES
Gastroenterology & Urology
26d
Cleared
Aug 05, 1999
UROSTYM BIOFEEDBACK AND STIMULATION PROBES
Gastroenterology & Urology
211d
Cleared
Jul 07, 1999
VISER PENILE TUMESCENCE MONITOR
Gastroenterology & Urology
70d
Cleared
Jun 05, 1997
ANO-RECTAL MANOMETRY OPTION, MODEL NUMBER UDS-ARM
Gastroenterology & Urology
302d
Cleared
Mar 30, 1995
CART, MODE NUMBER UDS-CART
Gastroenterology & Urology
86d