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ANGIOTEC SC 1221 SCAN CONVERTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850330
510(k) Type
Traditional
Applicant
ANGIOTEC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1985
Days to Decision
92 days

ANGIOTEC SC 1221 SCAN CONVERTER

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K850330
510(k) Type
Traditional
Applicant
ANGIOTEC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1985
Days to Decision
92 days