PATIENT LIFT— 510(k) K780684

Name: FDA 510(k) clearance K780684
Creator: U.S. Food and Drug Administration
Published: 1978-06-06

Substantially Equivalent

Orthopedic Equipment Co., Inc.

FDA 510(k) clearance K780684 for PATIENT LIFT, Substantially Equivalent on 1978-06-06. Applicant: Orthopedic Equipment Co., Inc.. Device class: 1.

Clearance details

Applicant: Orthopedic Equipment Co., Inc.
Product code: Code FSA
Device class: Class 1
Regulation: 21 CFR 880.5510
Advisory panel: General Hospital
Date received: 1978-04-24
Decision date: 1978-06-06
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K942807 — SURGICAL LIFT SHEET1994-08-02
K930625 — SANITAS PATIENT LIFT1993-09-13
K902141 — ANOLIFT - PORTABLE & ANOLIFT - GANTRY1990-09-12
K860837 — HOYER ONE-TOUCH POWER LIFTER1986-03-27
K851844 — MOLIFT1985-05-17

More clearances from Orthopedic Equipment Co., Inc.

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K834035 — UNIVERSAL SELF-ALIGNING ACETABULAR COM1984-06-19
K841189 — OEC/REZAIAN SPINAL FIXATOR1984-05-16
K800530 — SCHLEIN TRI-SURFACE ANKLE1980-04-02
K781445 — SPREADER1979-09-27
K790209 — FILTER SYSTEM, ALTNER DISPOSABLE1979-02-26

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.