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Pathfinder Endoscope Overtube with Balloon Device

Page Type
Cleared 510(K)
510(k) Number
K230801
510(k) Type
Traditional
Applicant
Neptune Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2023
Days to Decision
127 days
Submission Type
Summary

Pathfinder Endoscope Overtube with Balloon Device

Page Type
Cleared 510(K)
510(k) Number
K230801
510(k) Type
Traditional
Applicant
Neptune Medical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/28/2023
Days to Decision
127 days
Submission Type
Summary