meddevicedb.com FDA Device Reference

STERILE RUBBER BANDS

K834063 Traditional
Decision Date
1983-12-22
Sponsor / Applicant
Devon Industries, Inc.

Technical Specification

510(k) Submission ID K834063
Product Code LDQ
Medical Specialty / Panel General Hospital
Decision Date 1983-12-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE RUBBER BANDS received FDA 510(k) clearance under submission number K834063, 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 1983-12-22.

Classification & Regulation

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