Last synced on 14 November 2025 at 11:06 pm

DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132059
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2013
Days to Decision
114 days
Submission Type
Summary

DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K132059
510(k) Type
Traditional
Applicant
ADVANCED INSTRUMENTATIONS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2013
Days to Decision
114 days
Submission Type
Summary