Generic Medical Device, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K111219GMD UNIVERSAL URINARY INCONTINENCE SLINGJune 30, 2011
K083471GMD UNIVERSAL SLING, MODEL PRODUCT CODE 1010 AND 1020March 3, 2009
K070018UNIVERSAL SURGICAL MESH, MODEL 100April 27, 2007
K063429GMD UNIVERSAL CIRCUMCISION CLAMP, MODEL 200January 17, 2007