Vision Quest Industries, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
6
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K142236BioniCare Hand SystemMarch 23, 2015
K090532T.E.A.R. TECH3November 13, 2009
K072799TARGET STERILE ELECTRODEApril 24, 2008
K041092FAST START TENS, MODEL FS 3001July 1, 2004
K030507T.E.A.R. TECH3 MODEL #44TT03May 20, 2003
K982388SURGI STIMSeptember 14, 1998