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ULTRA-THIN DIAMOND BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K963397
510(k) Type
Traditional
Applicant
Boston Scientific Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1996
Days to Decision
88 days
Submission Type
Summary

ULTRA-THIN DIAMOND BALLOON DILATATION CATHETER

Page Type
Cleared 510(K)
510(k) Number
K963397
510(k) Type
Traditional
Applicant
Boston Scientific Corp
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/25/1996
Days to Decision
88 days
Submission Type
Summary