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CHISON DIGITAL ULTRASOUND SYSTEM, CONVEX PROBE, LINEAR PROBE, TRANSVAGINAL MICRO-CONVEX PROBE, TRANSRECTAL LINEAR PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112539
510(k) Type
Traditional
Applicant
LEIKER REGULATORY & QUALITY CONSULTING
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2012
Days to Decision
151 days
Submission Type
Summary

CHISON DIGITAL ULTRASOUND SYSTEM, CONVEX PROBE, LINEAR PROBE, TRANSVAGINAL MICRO-CONVEX PROBE, TRANSRECTAL LINEAR PROBE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K112539
510(k) Type
Traditional
Applicant
LEIKER REGULATORY & QUALITY CONSULTING
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/2012
Days to Decision
151 days
Submission Type
Summary