Product code MQX— General Hospital

ACUPUNCTURE NEEDLES

Classification name
Needle, Acupuncture, Single Use
Device class
Class 2
Regulation
21 CFR 880.5580
Advisory panel
General Hospital
Total cleared
91
First cleared
Most recent

Market context for product code MQX

FDA has cleared 91 devices under product code MQX between 1996 and 2017, filed by 52 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 MQX

Recent clearances under product code MQX

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