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MDI 2000 - PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K850791
510(k) Type
Traditional
Applicant
MICROMEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/1985
Days to Decision
113 days

MDI 2000 - PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K850791
510(k) Type
Traditional
Applicant
MICROMEDICAL DEVICES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/19/1985
Days to Decision
113 days