THE MURRAY MOBILIFT(TM)— 510(k) K895677

Name: FDA 510(k) clearance K895677
Creator: U.S. Food and Drug Administration
Published: 1990-10-26

Substantially Equivalent

Medical/Surgical Specialties, Ltd.

FDA 510(k) clearance K895677 for THE MURRAY MOBILIFT(TM), Substantially Equivalent on 1990-10-26. Applicant: Medical/Surgical Specialties, Ltd.. Device class: 2.

Clearance details

Applicant: Medical/Surgical Specialties, Ltd.
Product code: Code FNG
Device class: Class 2
Regulation: 21 CFR 880.5500
Advisory panel: General Hospital
Date received: 1989-09-20
Decision date: 1990-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Kalamazoo, MI, US

Download summary PDF View on FDA.gov ↗

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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.