meddevicedb.com FDA Device Reference

STERILE LABELS

K834062 Traditional
Decision Date
1984-02-04
Sponsor / Applicant
Devon Industries, Inc.

Technical Specification

510(k) Submission ID K834062
Product Code LDQ
Medical Specialty / Panel General Hospital
Decision Date 1984-02-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE LABELS received FDA 510(k) clearance under submission number K834062, sponsored by Devon Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1984-02-04.

Classification & Regulation

This clearance is catalogued under FDA product code LDQ , within the General Hospital review panel as a device.