Last synced on 14 November 2025 at 11:06 pm

ULTRAEXTEND USWS-900A V2.1 AND V3.1

Page Type
Cleared 510(K)
510(k) Number
K131822
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2013
Days to Decision
33 days
Submission Type
Summary

ULTRAEXTEND USWS-900A V2.1 AND V3.1

Page Type
Cleared 510(K)
510(k) Number
K131822
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MEDICAL SYSTEMS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/23/2013
Days to Decision
33 days
Submission Type
Summary