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Apieron, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
2
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K083617APIERON INSIGHT ENO SYSTEMJanuary 27, 2009
K073265APIERON INSIGHT EXHALED NITRIC OXIDE (ENO) SYSTEMMarch 14, 2008