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HARMAC BALLOON ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962829
510(k) Type
Traditional
Applicant
Harmac Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1997
Days to Decision
475 days
Submission Type
Statement

HARMAC BALLOON ANGIOGRAPHIC CATHETER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K962829
510(k) Type
Traditional
Applicant
Harmac Medical Products, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/16/1997
Days to Decision
475 days
Submission Type
Statement