Medical Device Manufacturer · US , Mchenry , IL

Verite - FDA 510(k) Cleared Devices

10 submissions · 9 cleared · Since 1979

Total

Cleared

Denied

Verite has 9 FDA 510(k) cleared neurology devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1979 to 1985.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Verite is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Verite

10 devices

1-10 of 10

Cleared Jul 09, 1985

MODEL 1000

K844727 · IPF

Physical Medicine · 217d

MODEL 811 VERI/TENS & PO

K840098 · GZJ

Neurology · 189d

Cleared Nov 17, 1982

VERIL/PPR PERSONAL PAIN RELIEVER #800

K822929 · GZJ

Neurology · 44d

Cleared Apr 29, 1982

MODEL 860-1 VERI/PROBE

Physical Medicine · 108d

Physical Medicine · 17d

Verite - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Verite

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