Product code KDQ— General Hospital

ABCO SUCTION CANISTER

Classification name
Bottle, Collection, Vacuum
Device class
Class 2
Regulation
21 CFR 880.6740
Advisory panel
General Hospital
Total cleared
48
First cleared
Most recent

Market context for product code KDQ

FDA has cleared 48 devices under product code KDQ between 1976 and 2008, 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 KDQ

Adverse events under product code KDQ

product code KDQ
Death
8
Malfunction
637
Total
645

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 KDQ

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