INFUS. SETS-9120-50 CM & 9121-100 CM,EXT— 510(k) K822775

Substantially Equivalent

Cardiac Pacemakers, Inc.

FDA 510(k) clearance K822775 for INFUS. SETS-9120-50 CM & 9121-100 CM,EXT, Substantially Equivalent on 1982-11-03. Applicant: Cardiac Pacemakers, Inc..

Clearance details

Applicant: Cardiac Pacemakers, Inc.
Product code: Code FPA
Advisory panel: General Hospital
Date received: 1982-09-14
Decision date: 1982-11-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: MN, US

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Adverse events under product code FPA

product code FPA

Death: 95
Injury: 14,421
Malfunction: 125,815
Other: 30
Total: 140,361

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.