Medical Device Manufacturer · CA , Mississauga

Laborie Medical Tech Corp. - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 1995

Recent clearances: UROSTYM BIOFEEDBACK AND STIMULATION ANAL/RECTAL PROBES, UROSTYM BIOFEEDBACK AND STIMULATION PROBES, VISER PENILE TUMESCENCE MONITOR

5

Total

5

Cleared

0

Denied

FDA 510(k) Regulatory Record - Laborie Medical Tech Corp. Gastroenterology & Urology ✕

5 devices

1-5 of 5

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