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BAXTER SENSOR CORONARY GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K923240
510(k) Type
Traditional
Applicant
BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1992
Days to Decision
83 days
Submission Type
Summary

BAXTER SENSOR CORONARY GUIDEWIRE

Page Type
Cleared 510(K)
510(k) Number
K923240
510(k) Type
Traditional
Applicant
BAXTER HEALTHCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/23/1992
Days to Decision
83 days
Submission Type
Summary