PEEPER— 510(k) K830395

Substantially Equivalent

Dupaco, Inc.

FDA 510(k) clearance K830395 for PEEPER, Substantially Equivalent on 1983-03-11. Applicant: Dupaco, Inc..

Clearance details

Applicant: Dupaco, Inc.
Product code: Code BYE
Advisory panel: Anesthesiology
Date received: 1983-02-07
Decision date: 1983-03-11
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Adverse events under product code BYE

product code BYE

Death: 5
Total: 5

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.