AQUACISER SYSTEM— 510(k) K890548

Substantially Equivalent

Aquaciser, Inc.

FDA 510(k) clearance K890548 for AQUACISER SYSTEM, Substantially Equivalent on 1989-02-13. Applicant: Aquaciser, Inc..

Clearance details

Applicant: Aquaciser, Inc.
Product code: Code ILJ
Advisory panel: Physical Medicine
Date received: 1989-02-03
Decision date: 1989-02-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Chicago, IL, US

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Adverse events under product code ILJ

product code ILJ

Death: 4
Total: 4

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.