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SIEMENS-ELEMA PULSE GENERATOR 668 B

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812610
510(k) Type
Traditional
Applicant
SIEMENS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/1981
Days to Decision
86 days

SIEMENS-ELEMA PULSE GENERATOR 668 B

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K812610
510(k) Type
Traditional
Applicant
SIEMENS CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/10/1981
Days to Decision
86 days