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QUANTIX/ND DEVICE

Page Type
Cleared 510(K)
510(k) Number
K023431
510(k) Type
Special
Applicant
CARDIOSONIX, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/13/2002
Days to Decision
29 days
Submission Type
Summary

QUANTIX/ND DEVICE

Page Type
Cleared 510(K)
510(k) Number
K023431
510(k) Type
Special
Applicant
CARDIOSONIX, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
11/13/2002
Days to Decision
29 days
Submission Type
Summary