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Akcess Medical Products, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
36
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K926374SILICONE CATHETER REPAIR KITSOctober 7, 1994
K925819AKCESS0CATH KITAugust 2, 1994
K925818AKCESS-CATHApril 5, 1994
K930630RIGHT ATRIAL CATHETERFebruary 7, 1994
K931120COAXIAL ACUTE CATHETERJanuary 14, 1994
K920634SPLITTABLE SHEATH INTRODUCER SETJanuary 14, 1994
K914936CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH SETApril 23, 1992
K920331RIGHT ATRIAL CATHETER KITSApril 22, 1992
K914826AKCESS-CATH KITApril 10, 1992
K915215CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATH. KITSMarch 27, 1992
K911333RIGHT ATRIAL CATHETERSSeptember 23, 1991
K910641INTRODUCER NEEDLESApril 29, 1991
K910502VESSEL DILATORSApril 29, 1991
K910501PERMANENT SILICONE CATHETERSApril 29, 1991
K910572INJECTION CAPSApril 29, 1991
K910321Y ADAPTORApril 16, 1991
K904139SINGLE LUMEN CATHETER KITSDecember 4, 1990
K904140SINGLE LUMEN CATHETERS, MODIFICATIONNovember 27, 1990
K904433DUAL LUMEN NEEDLESNovember 23, 1990
K902203TENCKHOFF PERITONEAL DIALYSIS KITAugust 1, 1990