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Columbus Instruments Intl. Corp.

FDA Regulatory Profile

Columbus Instruments Intl. Corp. appears in FDA public data with 0 recalls, 5 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 28, 1990.

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K895791OXYMAXMarch 28, 1990
K861543CARDIOMAX-IIMarch 10, 1987
K861100ISO-THERMEXMay 12, 1986
K782036TREMOR MONITORJanuary 23, 1979
K771718CARDIOTHERM-500XSeptember 28, 1977

FDA data resources