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QUANTIX OR VESSEL STABILIZER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K041180
510(k) Type
Special
Applicant
CARDIOSONIX, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/7/2004
Days to Decision
32 days
Submission Type
Summary

QUANTIX OR VESSEL STABILIZER DEVICE

Page Type
Cleared 510(K)
510(k) Number
K041180
510(k) Type
Special
Applicant
CARDIOSONIX, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
6/7/2004
Days to Decision
32 days
Submission Type
Summary