JYG — Curette, Ear Class I

FDA Device Classification

FDA product code JYG covers "Curette, Ear", a Class I medical device regulated under 21 CFR 874.4420. Submissions are reviewed by the Ear, Nose, Throat panel. At least 7 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
JYG
Device Class
Class I
Regulation Number
874.4420
Submission Type
510(k) Exempt
Review Panel
EN
Medical Specialty
Ear, Nose, Throat
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K932609Ear TechEAR CURETTEJul 21, 1993
K852039BionixFLEX-LOOP FLEXIBLE EAR CORETTEJun 11, 1985
K841354Treace MedicalCURETTEJul 6, 1984
K841001Premier Dental ProductsEAR CURETTE, VARIOUSMay 29, 1984
K823916Treace MedicalWAX CURETTE TIPJan 21, 1983
K822273KelleherENT CURRETTESAug 30, 1982
K822006KelleherOPERATIVE EAR CURRETTES & RELATED ITEMAug 12, 1982

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.