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Akers Research Corp.

FDA Regulatory Profile

Akers Research Corp. has 0 FDA recalls, 0 inspections, 3 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Jul 27, 1992

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances3Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 9, 2026Newest record Oct 28, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) Clearances

K-NumberDeviceDate
K920222HEALTHTEST ASSAY FOR ANTIBODY TO CYTOMEGALOVIRUSJul 27, 1992
K920220HEALTHTEST RHEUMATOID FACTOR ASSAYMar 13, 1992
K920221HEALTHTEST INFECTIOUS MONONUCLEOSIS ASSAYMar 13, 1992

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.