Last synced on 14 November 2025 at 11:06 pm

APLIO ARTIDA DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121577
510(k) Type
Special
Applicant
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2012
Days to Decision
23 days
Submission Type
Summary

APLIO ARTIDA DIAGNOSTIC ULTRASOUND SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K121577
510(k) Type
Special
Applicant
TOSHIBA MEDICAL SYSTEMS CORPORATION, JAPAN
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/22/2012
Days to Decision
23 days
Submission Type
Summary