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M2430 DIAGNOSTIC ULTRASOUND SYSTEM WITH THE 21420 TRANSDUCER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002397
510(k) Type
Traditional
Applicant
Agilent Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2000
Days to Decision
10 days
Submission Type
Summary

M2430 DIAGNOSTIC ULTRASOUND SYSTEM WITH THE 21420 TRANSDUCER

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K002397
510(k) Type
Traditional
Applicant
Agilent Technologies, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/17/2000
Days to Decision
10 days
Submission Type
Summary