Product code JYW— Ear, Nose, Throat

CALIBRATED TISSUE GRAFT PRESS

Classification name: Press, Vein
Device class: Class 1
Regulation: 21 CFR 874.4420
Advisory panel: Ear, Nose, Throat
Total cleared: 1
First cleared: 1982-09-09
Most recent: 1982-09-09

Market context for product code JYW

FDA has cleared 1 device under product code JYW, all in 1982, filed by 1 applicant company. 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.

Top applicants under product code JYW

Treace Medical, Inc.1 clearance

Recent clearances under product code JYW

K822368 — CALIBRATED TISSUE GRAFT PRESSTreace Medical, Inc.·1982-09-09

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