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SONICAID MODEL MERIDIAN 800

Page Type
Cleared 510(K)
510(k) Number
K902690
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/1991
Days to Decision
231 days

SONICAID MODEL MERIDIAN 800

Page Type
Cleared 510(K)
510(k) Number
K902690
510(k) Type
Traditional
Applicant
OXFORD MEDILOG, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/5/1991
Days to Decision
231 days