LIFELIFT MODELS ONE AND TWO— 510(k) K792601

Name: FDA 510(k) clearance K792601
Creator: U.S. Food and Drug Administration
Published: 1979-12-31

Substantially Equivalent

Corda Int'L Holiday, Inc.

FDA 510(k) clearance K792601 for LIFELIFT MODELS ONE AND TWO, Substantially Equivalent on 1979-12-31. Applicant: Corda Int'L Holiday, Inc.. Device class: 1.

Clearance details

Applicant: Corda Int'L Holiday, Inc.
Product code: Code FSA
Device class: Class 1
Regulation: 21 CFR 880.5510
Advisory panel: General Hospital
Date received: 1979-12-18
Decision date: 1979-12-31
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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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.