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ECLIPSE 2100(TM) MODEL 32, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K931101
510(k) Type
Traditional
Applicant
CARDIOGENES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1993
Days to Decision
198 days
Submission Type
Statement

ECLIPSE 2100(TM) MODEL 32, MODIFICATION

Page Type
Cleared 510(K)
510(k) Number
K931101
510(k) Type
Traditional
Applicant
CARDIOGENES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/25/1993
Days to Decision
198 days
Submission Type
Statement