Product code FPO— General Hospital

WHEELED STRETCHER

Classification name
Stretcher, Wheeled
Device class
Class 2
Regulation
21 CFR 880.6910
Advisory panel
General Hospital
Total cleared
50
First cleared
Most recent

Market context for product code FPO

FDA has cleared 50 devices under product code FPO between 1977 and 2011, filed by 32 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

last 15 years

Top applicants under product code FPO

Adverse events under product code FPO

product code FPO
Death
29
Injury
254
Malfunction
5,054
Other
10
Total
5,347

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 FPO

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