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ECTON LYNX ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K982800
510(k) Type
Traditional
Applicant
ECTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1998
Days to Decision
43 days
Submission Type
Summary

ECTON LYNX ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K982800
510(k) Type
Traditional
Applicant
ECTON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/22/1998
Days to Decision
43 days
Submission Type
Summary