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CANALIZER HYDROPHILIC GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K050873
510(k) Type
Traditional
Applicant
Medical Device Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2005
Days to Decision
50 days
Submission Type
Summary

CANALIZER HYDROPHILIC GUIDE WIRE

Page Type
Cleared 510(K)
510(k) Number
K050873
510(k) Type
Traditional
Applicant
Medical Device Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/26/2005
Days to Decision
50 days
Submission Type
Summary