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IMPLANT PROGRAM CARDIAC PULSE GEN W/MOD SET SCREW

Page Type
Cleared 510(K)
510(k) Number
K853206
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1985
Days to Decision
43 days

IMPLANT PROGRAM CARDIAC PULSE GEN W/MOD SET SCREW

Page Type
Cleared 510(K)
510(k) Number
K853206
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/12/1985
Days to Decision
43 days