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Baronova, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
3
Inspections
1
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K191078BAROnova Access Sheath KitJuly 22, 2019
K190985BAROnova Insufflation System, BAROnova Accessory KitMay 14, 2019
K172575BAROnova Retrieval Kit, BAROnova Overtube, BAROnova Endoscope CapJanuary 18, 2018