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PULSE GENERATOR, MODEL 240, EXTERNAL

Page Type
Cleared 510(K)
510(k) Number
K781327
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1978
Days to Decision
132 days

PULSE GENERATOR, MODEL 240, EXTERNAL

Page Type
Cleared 510(K)
510(k) Number
K781327
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/11/1978
Days to Decision
132 days