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Arrow X-Ray Corp.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
0
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K827069PODIOSCOPE BY ARROWFebruary 18, 1982
K820119PODIOSCOPE BY ARROWFebruary 18, 1982