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Accu-Line

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
4
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K831847JEJUNOSTOMY KITAugust 31, 1983
K831636PERCUTANEOUS INTRODUCER KITAugust 24, 1983
K831637ACCU-FLUSHJune 30, 1983
K830298ACCU-LINE SURGICAL MARKERJune 2, 1983