Last synced on 12 October 2025 at 8:21 pm

AFP SYSTEM PULSE GENERATOR MODEL 261/262

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822639
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1983
Days to Decision
170 days

AFP SYSTEM PULSE GENERATOR MODEL 261/262

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K822639
510(k) Type
Traditional
Applicant
PACESETTER SYSTEMS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1983
Days to Decision
170 days