MODEL 2001, MODIFICATION— 510(k) K905029

Substantially Equivalent

Medfusion, Inc.

FDA 510(k) clearance K905029 for MODEL 2001, MODIFICATION, Substantially Equivalent on 1990-12-24. Applicant: Medfusion, Inc..

Clearance details

Applicant: Medfusion, Inc.
Product code: Code FRN
Advisory panel: General Hospital
Date received: 1990-10-31
Decision date: 1990-12-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Duluth, GA, 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.