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ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATION

Page Type
Cleared 510(K)
510(k) Number
K922787
510(k) Type
Traditional
Applicant
ECHOCATH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1993
Days to Decision
211 days
Submission Type
Summary

ECHOMARK GUIDEWIRE WITH ULTRASONIC LOCALIZATION

Page Type
Cleared 510(K)
510(k) Number
K922787
510(k) Type
Traditional
Applicant
ECHOCATH, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/6/1993
Days to Decision
211 days
Submission Type
Summary