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PULSE GENERATOR MODEL 688

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833519
510(k) Type
Traditional
Applicant
BURDITT & CALKINS-SIEMENS-ELEMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1984
Days to Decision
111 days

PULSE GENERATOR MODEL 688

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K833519
510(k) Type
Traditional
Applicant
BURDITT & CALKINS-SIEMENS-ELEMA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/30/1984
Days to Decision
111 days