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Diagnostic Fixed Electrophysiology Lumen Catheter , Diagnostic Electrophysiology Cable

Page Type
Cleared 510(K)
510(k) Number
K183632
510(k) Type
Traditional
Applicant
Baylis Medical Company Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/7/2019
Days to Decision
163 days
Submission Type
Summary

Diagnostic Fixed Electrophysiology Lumen Catheter , Diagnostic Electrophysiology Cable

Page Type
Cleared 510(K)
510(k) Number
K183632
510(k) Type
Traditional
Applicant
Baylis Medical Company Inc.
Country
Canada
FDA Decision
Substantially Equivalent
Decision Date
6/7/2019
Days to Decision
163 days
Submission Type
Summary