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BATTERY FOR #229-01 PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K802040
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1980
Days to Decision
29 days

BATTERY FOR #229-01 PULSE GENERATOR

Page Type
Cleared 510(K)
510(k) Number
K802040
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/9/1980
Days to Decision
29 days