JYQ — Loop, Wire Class I

FDA Device Classification

FDA product code JYQ covers "Loop, Wire", a Class I medical device regulated under 21 CFR 874.4420. Submissions are reviewed by the Ear, Nose, Throat panel. At least 2 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
JYQ
Device Class
Class I
Regulation Number
874.4420
Submission Type
Review Panel
EN
Medical Specialty
Ear, Nose, Throat
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K890221kinetic medical productsMICROSURGICAL WIRE LOOPJanuary 27, 1989
K870761treace medicalEAR LOOPMarch 3, 1987