Last synced on 25 November 2022 at 11:04 pm

CRE PULMONARY BALLOON DILATATION CATHETER, MODELS K00550300, M00550310, M00550320, M00550330, M00550340, M00550350

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023337
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2002
Days to Decision
42 days
Submission Type
Summary

CRE PULMONARY BALLOON DILATATION CATHETER, MODELS K00550300, M00550310, M00550320, M00550330, M00550340, M00550350

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023337
510(k) Type
Traditional
Applicant
BOSTON SCIENTIFIC CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/18/2002
Days to Decision
42 days
Submission Type
Summary