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BAROnova Retrieval Kit, BAROnova Overtube, BAROnova Endoscope Cap

Page Type
Cleared 510(K)
510(k) Number
K172575
510(k) Type
Traditional
Applicant
BAROnova, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2018
Days to Decision
143 days
Submission Type
Summary

BAROnova Retrieval Kit, BAROnova Overtube, BAROnova Endoscope Cap

Page Type
Cleared 510(K)
510(k) Number
K172575
510(k) Type
Traditional
Applicant
BAROnova, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2018
Days to Decision
143 days
Submission Type
Summary