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CORDIS MULTIFILAR PERVENOUS VENTRIC. LD

Page Type
Cleared 510(K)
510(k) Number
K810202
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/1981
Days to Decision
13 days

CORDIS MULTIFILAR PERVENOUS VENTRIC. LD

Page Type
Cleared 510(K)
510(k) Number
K810202
510(k) Type
Traditional
Applicant
CORDIS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/1981
Days to Decision
13 days