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subpart-d—cardiovascular-prosthetic-devices/

COMMAND P5(BIPOLAR PULSE GENERATOR)

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K811402
510(k) Type: Traditional
Applicant: CARDIAC PACEMAKERS, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 7/27/1981
Days to Decision: 70 days

FDA Browser

subpart-d—cardiovascular-prosthetic-devices/

COMMAND P5(BIPOLAR PULSE GENERATOR)

Page Type: Cleared 510(K)
PDF: FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number: K811402
510(k) Type: Traditional
Applicant: CARDIAC PACEMAKERS, INC.
Country: United States
FDA Decision: Substantially Equivalent
Decision Date: 7/27/1981
Days to Decision: 70 days