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PACESETTER/SIEMENS PULSE GENERA W/VS-1 HEAD CAVITY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861422
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/1986
Days to Decision
71 days

PACESETTER/SIEMENS PULSE GENERA W/VS-1 HEAD CAVITY

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K861422
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/26/1986
Days to Decision
71 days