Product code KZD— General Hospital

PRESSURE INFUSER

Classification name
Infusor, Pressure, For I.V. Bags
Device class
Class 1
Regulation
21 CFR 880.5420
Advisory panel
General Hospital
Total cleared
35
First cleared
Most recent

Market context for product code KZD

FDA has cleared 35 devices under product code KZD between 1976 and 1998, filed by 31 applicant companies. No FDA device recalls reference this product code. Class I devices are low-risk and subject to FDA general controls; many Class I device types are exempt from 510(k) premarket notification.

Clearances per year

last 15 years

Top applicants under product code KZD

Adverse events under product code KZD

product code KZD
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 KZD

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