Last synced on 30 May 2025 at 11:05 pm

QUANTIX/ND DEVICE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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