Medical Device Manufacturer · US , Irvine , CA

American Imex - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1986

Total

Cleared

Denied

American Imex has 11 FDA 510(k) cleared neurology devices. Based in Irvine, US.

Historical record: 11 cleared submissions from 1986 to 2004.

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

American Imex 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 - American Imex

11 devices

1-11 of 11

ULTIMA XS, MODIFICATION

K912289 · GZJ

Neurology · 183d

Cleared Nov 06, 1989

ULTIMA XS MICROCURRENT TENS

American Imex - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - American Imex

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