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BIOTEQ ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K102633
510(k) Type
Traditional
Applicant
BIOTEQUE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2011
Days to Decision
361 days
Submission Type
Summary

BIOTEQ ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
510(k) Number
K102633
510(k) Type
Traditional
Applicant
BIOTEQUE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/2011
Days to Decision
361 days
Submission Type
Summary