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Astro-Med, Inc.

FDA Regulatory Profile

Astro-Med, Inc. has 0 FDA recalls, 0 inspections, 13 510(k) clearances and 0 compliance actions on record.

Latest 510(k)
Dec 24, 2008

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Oct 23, 2026Not statedCurrent
510(k) clearances13Oct 4, 2026Not statedCurrent
Inspections0Oct 26, 2026Not statedCurrent
Compliance actions0Oct 23, 2026Not statedCurrent

Recent 510(k) Clearances

K-NumberDeviceDate
K081551TWIN NEUROTRAC-IIIDec 24, 2008
K050425AURA-PSGOct 20, 2005
K033978ADAMFeb 18, 2004
K970951GRASS BRAINWAVE SOFTWAREMay 19, 1997
K963669GRASS MODEL 15 NEURODATA AMPLIFIER SYSTEMDec 12, 1996
K934644K3 SYSTEMNov 1, 1994
K912929DASH IVAug 13, 1991
K896164ASC-954 INTEGRATOR AMPLIFIERJan 22, 1990
K894295ASTRO-MED ASC-951 PRESSURE PROCESSORJan 18, 1990
K894736MT96000 PAPER CHART RECORDERDec 13, 1989
K894735ASC-952 PHYSIOLOGICAL AMPLIFIERSep 18, 1989
K894161ASC-950 ECG AMPLIFIERAug 3, 1989
K892067MT9000 CHART RECORDERJun 5, 1989

FDA data resources