Last synced on 14 November 2025 at 11:06 pm

ECLIPSE 2100

Page Type
Cleared 510(K)
510(k) Number
K955006
510(k) Type
Traditional
Applicant
CARDIOGENES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1996
Days to Decision
77 days
Submission Type
Summary

ECLIPSE 2100

Page Type
Cleared 510(K)
510(k) Number
K955006
510(k) Type
Traditional
Applicant
CARDIOGENES
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/17/1996
Days to Decision
77 days
Submission Type
Summary