Mpathy Medical Devices, Ltd.

FDA Regulatory Profile

Mpathy Medical Devices, Ltd. appears in FDA public data with 0 recalls, 7 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 12, 2009.

Summary

Total Recalls
0
510(k) Clearances
7
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K092203OMNISURE URETHRAL SLING, MODEL OTK52August 12, 2009
K092207RESTORELLE POLYPROPYLENE MESHAugust 4, 2009
K091180MINITAPE URETHRAL SLINGJuly 14, 2009
K073647MINITAPE EXTRA URETHRAL SLINGMarch 3, 2008
K073646MINITAPE URETHRAL SLINGFebruary 25, 2008
K053361MODIFICATION TO: MINIMESH POLYPROPYLENE MESHFebruary 6, 2006
K041632MINIMESH POLYPROPYLENE MESHNovember 17, 2004