HUMAPEN AND HUMAPEN ERGO— 510(k) K982842

Substantially Equivalent

Eli Lilly and Co.

FDA 510(k) clearance K982842 for HUMAPEN AND HUMAPEN ERGO, Substantially Equivalent on 1998-09-25. Applicant: Eli Lilly and Co..

Clearance details

Applicant: Eli Lilly and Co.
Product code: Code FMF
Advisory panel: General Hospital
Date received: 1998-08-12
Decision date: 1998-09-25
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Indianapolis, IN, US

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Adverse events under product code FMF

product code FMF

Death: 15
Injury: 2,263
Malfunction: 29,722
Other: 17
Total: 32,017

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.