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INTRACARDIAC SUMP 12010

Page Type
Cleared 510(K)
510(k) Number
K850385
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1985
Days to Decision
87 days

INTRACARDIAC SUMP 12010

Page Type
Cleared 510(K)
510(k) Number
K850385
510(k) Type
Traditional
Applicant
DLP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/29/1985
Days to Decision
87 days