North American Instrument Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
28
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K960801SELECTOR ANGIOGRAPHIC CATHETER (VARIOUS MODELS)March 29, 1996
K955554HEMO-VALVEMarch 4, 1996
K960310EPIC INTRODUCER SHEATHFebruary 7, 1996
K922552MORSE(R) ANGIOGRAPHIC CATHETERSMarch 3, 1993
K915078MORSE HEMOSTATIC CATHETER INTRODUCER SETJune 10, 1992
K905208MORSE ANESTHESIAJanuary 10, 1992
K912961MORSE VASCULAR INTRODUCER SETSeptember 11, 1991
K910764THE PERCEPTOR(TM) STAND ALONE TRANSDUCERApril 22, 1991
K903493NAMIC CONTRAST SAVINGS DELIVERY SYSTEMMarch 26, 1991
K904275MORSE BALLOON INFLATION DEVICEJanuary 3, 1991
K903606GUIDEWIRE TORQUE DEVICE AND GUIDEWIRE INTRODUCERSeptember 27, 1990
K902472MORSE DT MANIFOLDAugust 23, 1990
K900652NAMIC PTCA Y-ADAPTORJune 26, 1990
K896087PALESTRANT IRRIGATION AND DRAINAGE SETNovember 3, 1989
K890580LIPID STOPCOCKApril 19, 1989
K885090HOMER MAMMALOK LOCALIZATION SHIELDFebruary 14, 1989
K884408NAMIC DUAL BACKCHECK VALVEJanuary 12, 1989
K873955NAMIC ANGIOGRAPHIC SYRINGEFebruary 5, 1988
K873954NAMIC HAWKINS UNIVERSAL DRAINAGE SETJanuary 29, 1988
K871377NAMIC COURNAND STYLE INTRODUCER NEEDLEMay 7, 1987