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Alimed, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
11
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K963527UNIVERSAL ECONO-STRAP, QUALCRAFT UNIVERSAL STRAPSOctober 31, 1996
K963528ALIMED POSITIONING 7 SAFETY STRAPS (THREE TYPES), UNIVERSAL CR/MRI WIDE BODY STRAP, UNIVERSAL CT SCAOctober 29, 1996
K963526STRAP WEDGEOctober 28, 1996
K920487MINI VIBRATORFebruary 18, 1992
K840156PROTECTA COAT SPONGESMarch 23, 1984
K822650SUPER DONUTSeptember 30, 1982
K822651TOTAL FINGER FLEXION SPLINTSeptember 17, 1982
K820516ARTERIAL CANALIZATION DEVICEApril 15, 1982
K820517CONSTRUCTA FOAMMarch 10, 1982
K801743PLASTAZOTE SHOEAugust 7, 1980
K791189ECHO CARDIOGRAM PADJuly 17, 1979