CENTURY BATHING SYSTEM— 510(k) K811901

Name: FDA 510(k) clearance K811901
Creator: U.S. Food and Drug Administration
Published: 1981-07-23

Substantially Equivalent

Century Manufacturing Co.

FDA 510(k) clearance K811901 for CENTURY BATHING SYSTEM, Substantially Equivalent on 1981-07-23. Applicant: Century Manufacturing Co.. Device class: 2.

Clearance details

Applicant: Century Manufacturing Co.
Product code: Code FNG
Device class: Class 2
Regulation: 21 CFR 880.5500
Advisory panel: General Hospital
Date received: 1981-07-01
Decision date: 1981-07-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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More clearances from Century Manufacturing Co.

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K912769 — PATIENT LIFT AND TRANSPORT1991-10-02
K904106 — SPA SHELL1990-09-18
K844871 — CENTURY SAF-LIFT SCALE1985-02-08
K844872 — CENTURY SCALE1985-02-08
K830633 — LIC TILT BED1983-03-10

Adverse events under product code FNG

product code FNG

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.