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MODIFICATION TO ATLANTIS SR PRO 2 AND SR PRO CORONARY IMAGING CATHETERS, MODEL 39014 AND 38942

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063312
510(k) Type
Special
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2006
Days to Decision
28 days
Submission Type
Summary

MODIFICATION TO ATLANTIS SR PRO 2 AND SR PRO CORONARY IMAGING CATHETERS, MODEL 39014 AND 38942

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K063312
510(k) Type
Special
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/30/2006
Days to Decision
28 days
Submission Type
Summary