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C2 CryoBalloon Catheter (Pear), C2 CryoBalloon (Standard), C2 CryoBalloon Controller, C2 CryoBalloon Foot Pedal, C2 CryoBalloon Cartridge

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190194
510(k) Type
Traditional
Applicant
PENTAX Medical, A Division of PENTAX of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2019
Days to Decision
116 days
Submission Type
Summary

C2 CryoBalloon Catheter (Pear), C2 CryoBalloon (Standard), C2 CryoBalloon Controller, C2 CryoBalloon Foot Pedal, C2 CryoBalloon Cartridge

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K190194
510(k) Type
Traditional
Applicant
PENTAX Medical, A Division of PENTAX of America, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/31/2019
Days to Decision
116 days
Submission Type
Summary