MODEL K110SX CENTRIFUGE— 510(k) K861146

Substantially Equivalent

Jouan S.A.

FDA 510(k) clearance K861146 for MODEL K110SX CENTRIFUGE, Substantially Equivalent on 1986-05-05. Applicant: Jouan S.A..

Clearance details

Applicant: Jouan S.A.
Product code: Code JQC
Advisory panel: Clinical Chemistry
Date received: 1986-03-26
Decision date: 1986-05-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Winchester, VA, US

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Adverse events under product code JQC

product code JQC

Other: 1
Total: 1

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.