Product code FNG— General Hospital

A.C. POWER PATIENT LIFT

Classification name
Lift, Patient, Ac-Powered
Device class
Class 2
Regulation
21 CFR 880.5500
Advisory panel
General Hospital
Total cleared
21
First cleared
Most recent

Market context for product code FNG

FDA has cleared 21 devices under product code FNG between 1980 and 2012, filed by 16 applicant companies. No FDA device recalls reference this product code. Class II devices are moderate-risk and subject to general and special controls; most reach market through 510(k) clearance by demonstrating substantial equivalence to a predicate device.

Clearances per year

Top applicants under product code FNG

Adverse events under product code FNG

product code FNG
Death
4
Total
4

Source: openFDA MAUDE database, through . Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Recent clearances under product code FNG

Data sourced from openFDA. This site is unofficial and independent of the FDA.