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BICORE SMARTCATH INTRATRACHEAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K935788
510(k) Type
Traditional
Applicant
BICORE MONITORING SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1995
Days to Decision
574 days
Submission Type
Summary

BICORE SMARTCATH INTRATRACHEAL CATHETER

Page Type
Cleared 510(K)
510(k) Number
K935788
510(k) Type
Traditional
Applicant
BICORE MONITORING SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/3/1995
Days to Decision
574 days
Submission Type
Summary