Medical Device Manufacturer · US , Mchenry , IL

Aktis Corp. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1984

2

Total

2

Cleared

0

Denied

FDA 510(k) Regulatory Record - Aktis Corp. Toxicology ✕

1 devices

1-1 of 1

Cleared Aug 16, 1984

IMMPULSE DIGOXIN ASSAY REAGENTS

Toxicology · 44d

Data Source

Sourced from the FDA 510(k) public files . 175,730 total devices indexed.

Last updated: Apr 28, 2026