BATTERY POWERED PATIENT LIFT— 510(k) K840997

Name: FDA 510(k) clearance K840997
Creator: U.S. Food and Drug Administration
Published: 1984-04-17

Substantially Equivalent

Invacare Corp.

FDA 510(k) clearance K840997 for BATTERY POWERED PATIENT LIFT, Substantially Equivalent on 1984-04-17. Applicant: Invacare Corp.. Device class: 1.

Clearance details

Applicant: Invacare Corp.
Product code: Code FSA
Device class: Class 1
Regulation: 21 CFR 880.5510
Advisory panel: General Hospital
Date received: 1984-03-08
Decision date: 1984-04-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Elyria, OH, US

Download summary PDF View on FDA.gov ↗

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K902141 — ANOLIFT - PORTABLE & ANOLIFT - GANTRY1990-09-12
K860837 — HOYER ONE-TOUCH POWER LIFTER1986-03-27
K851844 — MOLIFT1985-05-17

More clearances from Invacare Corp.

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K071928 — THE INVACARE FLYER, MODEL IPC 1002007-12-12
K070321 — TWILIGHT FULL FACE MASK2007-04-30
K062402 — EASYSTAND EVOLV2006-09-21
K061874 — INVACARE'S TWILIGHT II NASAL MASKS2006-09-05
K033819 — INVACARE 3G TARSYS2004-06-04

Adverse events under product code FSA

product code FSA

Death: 101
Injury: 767
Malfunction: 1,173
Other: 1
Total: 2,042

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.