Last synced on 25 January 2026 at 3:41 am

Q LAB QUANTIFICATION SOFTWARE WITH STRAIN RATE QUANTIFICATION PLUG-IN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023877
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2002
Days to Decision
32 days
Submission Type
Summary

Q LAB QUANTIFICATION SOFTWARE WITH STRAIN RATE QUANTIFICATION PLUG-IN

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K023877
510(k) Type
Traditional
Applicant
Philips Ultrasound, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/23/2002
Days to Decision
32 days
Submission Type
Summary