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ANGIOSCOPE FOR PULMONARY ARTERY USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882658
510(k) Type
Traditional
Applicant
WASHINGTON REGULATORY SERVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1989
Days to Decision
211 days

ANGIOSCOPE FOR PULMONARY ARTERY USE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K882658
510(k) Type
Traditional
Applicant
WASHINGTON REGULATORY SERVICES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/1989
Days to Decision
211 days