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THINLITH II PULSE GNEERATOR MODEL 227-05

Page Type
Cleared 510(K)
510(k) Number
K810386
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1981
Days to Decision
28 days

THINLITH II PULSE GNEERATOR MODEL 227-05

Page Type
Cleared 510(K)
510(k) Number
K810386
510(k) Type
Traditional
Applicant
INTERMEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/13/1981
Days to Decision
28 days