Medical Device Manufacturer · US , Mchenry , IL

Verite - FDA 510(k) Cleared Devices

10 submissions · 9 cleared · Since 1979

10

Total

9

Cleared

0

Denied

FDA 510(k) Regulatory Record - Verite Neurology ✕

7 devices

1-7 of 7

Cleared Nov 28, 1984

MODEL 800-A VERI/PPR

Neurology · 323d

Cleared Jul 17, 1984

MODEL 811 VERI/TENS & PO

Neurology · 189d

Cleared Nov 17, 1982

VERIL/PPR PERSONAL PAIN RELIEVER #800

Neurology · 44d

Cleared Apr 29, 1982

MODEL 860-1 VERI/PROBE

Neurology · 51d

Cleared Jan 19, 1982

VERI/DFS TM #817

Neurology · 35d

Cleared Jul 30, 1981

Neurology · 78d

Cleared Aug 22, 1979

MODEL 810 VERI/TGS

Neurology · 57d