DeviceClearance

Product code LZH— General Hospital

AMBULATORY ENTERAL NUTRITION PUMP

Classification name
Pump, Infusion, Enteral
Device class
Class 2
Regulation
21 CFR 880.5725
Advisory panel
General Hospital
Total cleared
34
First cleared
Most recent

Market context for product code LZH

FDA has cleared 34 devices under product code LZH between 1987 and 2026, filed by 25 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 LZH

Adverse events under product code LZH

product code LZH
Death
12
Malfunction
4,186
Total
4,198

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 LZH

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