INVALIFT— 510(k) K910830

Name: FDA 510(k) clearance K910830
Creator: U.S. Food and Drug Administration
Published: 1992-06-09

Substantially Equivalent

American Invalift Corp.

FDA 510(k) clearance K910830 for INVALIFT, Substantially Equivalent on 1992-06-09. Applicant: American Invalift Corp.. Device class: 2.

Clearance details

Applicant: American Invalift Corp.
Product code: Code FRZ
Device class: Class 2
Regulation: 21 CFR 880.6775
Advisory panel: General Hospital
Date received: 1991-02-27
Decision date: 1992-06-09
Decision: Substantially Equivalent
Clearance type: Traditional
Location: White Plains, NY, US

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Adverse events under product code FRZ

product code FRZ

Other: 1
Total: 1

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.