Product code NFQ— Dental

ARTHROPHONOMETER

Classification name: Device, Dental Sonography, For Monitoring Jaw Sounds
Device class: Class 1
Regulation: 21 CFR 872.2050
Advisory panel: Dental
Total cleared: 4
First cleared: 1987-01-07
Most recent: 1997-04-02

Market context for product code NFQ

FDA has cleared 4 devices under product code NFQ between 1987 and 1997, filed by 3 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

19971 clearance
19912 clearances
19871 clearance

Top applicants under product code NFQ

Myo-Tronics, Inc.2 clearances
Bioresearch1 clearance
Arthrotek, Inc.1 clearance

Recent clearances under product code NFQ

K970116 — ESG-1 ELECTROSONOGRAM (ESG-1)Myo-Tronics, Inc.·1997-04-02
K905657 — SONOPAK/QS, SONOPAKBioresearch·1991-05-15
K905449 — ELECTROSONOGRAM ESG-1Myo-Tronics, Inc.·1991-04-26
K862286 — ARTHROPHONOMETERArthrotek, Inc.·1987-01-07

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