Medical Device Manufacturer · US , Mchenry , IL

Kemble Instruments, Inc. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1982

Total

Cleared

Denied

Kemble Instruments, Inc. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1982 to 1984. Primary specialty: Chemistry.

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

FDA 510(k) Regulatory Record - Kemble Instruments, Inc.

9 devices

1-9 of 9

KEMTEK 400 RIA GAMMA COUNTER

KEMTEK 103 RIA GAMMA COUNTER

K832735 · JJJ

Chemistry · 56d

Cleared Sep 29, 1983

KEMTEK 104 RIA GAMMA COUNTER

THYRO-COUNT THYROID UPTAKE SYSTEM 90IZD PROBE

Kemble Instruments, Inc. - FDA 510(k) Cleared Devices

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