Medical Device Manufacturer · US , Mchenry , IL

V-Tech, Inc. - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 1982

Total

Cleared

Denied

V-Tech, Inc. has 22 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 22 cleared submissions from 1982 to 1991. Primary specialty: Chemistry.

Browse the FDA 510(k) cleared devices submitted by V-Tech, Inc. Filter by specialty or product code using the sidebar.

V-Tech, Inc. 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 - V-Tech, Inc.

22 devices

1-12 of 22

TARGET(TM) CANNABINOIDS-V TEST

K910892 · LDJ

Toxicology · 30d

Cleared Apr 03, 1991

TARGET(TM) CANNABINOIDS-R TEST

K910893 · LDJ

Toxicology · 30d

Cleared Mar 21, 1991

TARGET AMPHETAMINE/METHAMPHETAMINE-R (READER METH)

K910739 · DKZ

Toxicology · 28d

Cleared Mar 19, 1991

TARGET COCAINE METABOLITE-R

K910122 · KLN

Immunology · 67d

Cleared Mar 19, 1991

TARGET COCAINE METABOLITE-V

K910123 · KLN

Toxicology · 67d

Cleared Mar 19, 1991

TARGET AMPHETAMINE/METHAMPHETAMINE-V (VISUAL METH)

K910738 · DKZ

Toxicology · 26d

Cleared Oct 22, 1990

TARGET(TM) HOG ONE STEP

TARGET(TM) QUANTITATIVE HCG

K890131 · JHI

Chemistry · 56d

V-Tech, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - V-Tech, Inc.

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