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MEDIMOD(TM), MODEL 8900

Page Type
Cleared 510(K)
510(k) Number
K890705
510(k) Type
Traditional
Applicant
MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1989
Days to Decision
27 days

MEDIMOD(TM), MODEL 8900

Page Type
Cleared 510(K)
510(k) Number
K890705
510(k) Type
Traditional
Applicant
MEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/9/1989
Days to Decision
27 days