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LYNX ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K991872
510(k) Type
Traditional
Applicant
ECTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1999
Days to Decision
15 days
Submission Type
Summary

LYNX ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K991872
510(k) Type
Traditional
Applicant
ECTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/16/1999
Days to Decision
15 days
Submission Type
Summary