Last synced on 14 November 2025 at 11:06 pm

QUANTIX/OR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K030357
510(k) Type
Traditional
Applicant
CARDIOSONIX, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/20/2003
Days to Decision
198 days
Submission Type
Summary

QUANTIX/OR DEVICE

Page Type
Cleared 510(K)
510(k) Number
K030357
510(k) Type
Traditional
Applicant
CARDIOSONIX, LTD.
Country
Israel
FDA Decision
Substantially Equivalent
Decision Date
8/20/2003
Days to Decision
198 days
Submission Type
Summary