Product code JYM— Ear, Nose, Throat

ARMSTRONG V TUBE SUCTION INSERTER

Classification name: Inserter, Myringotomy Tube
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Total cleared: 4
First cleared: 1982-09-07
Most recent: 1993-01-28

Market context for product code JYM

FDA has cleared 4 devices under product code JYM between 1982 and 1993, 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

19931 clearance
19871 clearance
19822 clearances

Top applicants under product code JYM

Recent clearances under product code JYM

K924901 — DEANS DISPOSABLE T-TUBE INSERTERExmoor Plastics , Ltd.·1993-01-28
K870978 — T-TUBE INSERTERSur-Med Instruments, Inc.·1987-03-19
K822349 — ARMSTRONG V TUBE SUCTION INSERTERTreace Medical, Inc.·1982-09-13
K822348 — TYTAN TUBE INSERTERTreace Medical, Inc.·1982-09-07

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