CASCADE BATH, MODEL 6900— 510(k) K012057

Substantially Equivalent

Penner Manufacturing, Inc.

FDA 510(k) clearance K012057 for CASCADE BATH, MODEL 6900, Substantially Equivalent on 2001-07-19. Applicant: Penner Manufacturing, Inc..

Clearance details

Applicant: Penner Manufacturing, Inc.
Product code: Code ILJ
Advisory panel: Physical Medicine
Date received: 2001-07-02
Decision date: 2001-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Ohaha, NE, 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.