Last synced on 14 November 2025 at 11:06 pm

MODEL SONICAID AXIS

Page Type
Cleared 510(K)
510(k) Number
K912890
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1992
Days to Decision
192 days
Submission Type
Statement

MODEL SONICAID AXIS

Page Type
Cleared 510(K)
510(k) Number
K912890
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/1992
Days to Decision
192 days
Submission Type
Statement