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CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920822
510(k) Type
Traditional
Applicant
SIEMENS-PACESETTER, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
1/22/1993
Days to Decision
333 days
Submission Type
Summary

CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K920822
510(k) Type
Traditional
Applicant
SIEMENS-PACESETTER, INC.
Country
United States
FDA Decision
Substantially Equivalent - PostMarket Surveillance Required
Decision Date
1/22/1993
Days to Decision
333 days
Submission Type
Summary