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Cutler Medical Instruments

FDA Regulatory Profile

Cutler Medical Instruments has 0 FDA recalls, 0 inspections, 2 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Cutler Medical Instruments".

Latest 510(k)
Jul 11, 1986

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances2Nov 8, 2026File dated Nov 2, 2026Current
Inspections0Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Recent 510(k) clearances

2 510(k) clearances from Dec 27, 1985 to Jul 11, 1986.

K-NumberDeviceDate
K862343VACUUM HANDLE MODEL I/A - 1Jul 11, 1986
K854054PLACIDO DISCDec 27, 1985

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FDA data resources

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