Last synced on 14 November 2025 at 11:06 pm

MODIFIED RADIUS - MODEL NUMBER MM 5000

Page Type
Cleared 510(K)
510(k) Number
K871727
510(k) Type
Traditional
Applicant
ULTRASONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1987
Days to Decision
155 days

MODIFIED RADIUS - MODEL NUMBER MM 5000

Page Type
Cleared 510(K)
510(k) Number
K871727
510(k) Type
Traditional
Applicant
ULTRASONIX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/30/1987
Days to Decision
155 days