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CARDIAC PULSE GENERATOR, MODEL 150L

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772026
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1977
Days to Decision
7 days

CARDIAC PULSE GENERATOR, MODEL 150L

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K772026
510(k) Type
Traditional
Applicant
TELECTRONICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/3/1977
Days to Decision
7 days