INFUSION SETS MODELS 9120,9121,9125, 9122 & 9123— 510(k) K852060

Substantially Equivalent

Cardiac Pacemakers, Inc.

FDA 510(k) clearance K852060 for INFUSION SETS MODELS 9120,9121,9125, 9122 & 9123, Substantially Equivalent on 1985-06-07. Applicant: Cardiac Pacemakers, Inc..

Clearance details

Applicant: Cardiac Pacemakers, Inc.
Product code: Code FRN
Advisory panel: General Hospital
Date received: 1985-05-09
Decision date: 1985-06-07
Decision: Substantially Equivalent
Clearance type: Traditional
Location: St. Paul, MN, US

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Adverse events under product code FRN

product code FRN

Death: 540
Injury: 6,178
Malfunction: 1,464,165
Other: 52
Total: 1,470,935

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.