DeviceClearance

Product code QNQ— General Hospital

FEELject LDV (Low dead volume) syringe

Classification name
Low Dead Space Piston Syringe
Device class
Class 2
Regulation
21 CFR 880.5860
Advisory panel
General Hospital
Total cleared
12
First cleared
Most recent

FDA classification definition

“A low dead space syringe is a piston syringe designed to reduce medication waste. The device consists of a calibrated hollow barrel, a moveable plunger, and may include a needle. The device can be used by health care professions or for self-injection by the patient.”

— U.S. Food and Drug Administration, device classification record for product code QNQ under 21 CFR 880.5860, via openFDA

Market context for product code QNQ

FDA has cleared 12 devices under product code QNQ between 2021 and 2026, filed by 10 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 QNQ

Recent clearances under product code QNQ

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