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QNQClass II

Low Dead Space Piston Syringe

21 CFR 880.5860 / General Hospital

QNQ is the FDA product code for Low Dead Space Piston Syringe, a class II device type, regulated under 21 CFR 880.5860. FDA's definition for this code reads: "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". As of , FDA records hold 12 510(k) clearances under this code, the most recent dated , and no recalls.

Classification record

Product code
QNQ
Device name
Low Dead Space Piston Syringe
FDA 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.
Regulation
21 CFR 880.5860
Device class
Class II
Review panel
General Hospital
Submission type
510(k)
Implant
No
Life sustaining or supporting
No
GMP exempt
No
Third party review eligible
No
Ingested clearances
12
Ingested recalls
0

Clearances, product code QNQ

By decision year
12 clearances under product code QNQ with a decision year between 2021 and 2026, 2024 the highest year at 4.
Show the numbers
510(k) clearances under FDA product code QNQ by decision year
YearClearances
20211
20222
20232
20244
20252
20261

Applicants with the most clearances

Product code QNQ

Companies listing this code with FDA

Companies whose registered establishments list this code

12 of 15 companies shown, in name order