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VESSEL OCCLUDER

Page Type
Cleared 510(K)
510(k) Number
K800074
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/1980
Days to Decision
14 days

VESSEL OCCLUDER

Page Type
Cleared 510(K)
510(k) Number
K800074
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/1980
Days to Decision
14 days