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Analytical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
57
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K924814API 20E/UNISCEPT 20EMarch 11, 1993
K923684API UNISCEPT MIC/TYPE 2 AND 3 AND MICRO MICDecember 3, 1992
K922926API UNISCEPT KB/TYPE 2 AND 3October 13, 1992
K901559MODIFICATION TO API UNISCEPT 20GPSeptember 10, 1990
K901390DMAC INDOLE REAGENTApril 16, 1990
K895796API UNISCEPT KBNovember 13, 1989
K884510MODIFICATION MICRO-MICNovember 22, 1988
K884509MODIFICATION MIC/API UNISCEPT(R)November 22, 1988
K880598MODIFICATIONS TO API UNISCEPT (R) KBMarch 23, 1988
K874466API UNISCEPT(R) MICRO-MIC(R) SYSTEM/UNISCEPT MICDecember 9, 1987
K865062ALADIN (TM)March 25, 1987
K870663API UNISCEPT(R) MICRO-MIC(R) SYSTEM/UNISCEPT(R)MICMarch 23, 1987
K864891API UNISCEPT (TM) KBFebruary 20, 1987
K862543DYNEX CO2/2000, CO2 ANALYZERJuly 15, 1986
K860369API UNISCEPT MICRO-MIC CEFTRIAXONE/UNISCEPT MICMarch 11, 1986
K853544QUAD FERM +September 5, 1985
K850982CTAPI - NEISSERA SCREENMarch 29, 1985
K850347API UNISCEPT KBMarch 26, 1985
K844159API UNISCEPT MIC 100ULDecember 14, 1984
K843360ARTAP ARTERIAL BLOOD SAMPLING DEVICEOctober 31, 1984