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CITOJECT CARTRIDGE SYRINGE

K842006 Class II Traditional
Decision Date
1984-07-16
Sponsor / Applicant
Miles Laboratories, Inc.

Technical Specification

510(k) Submission ID K842006
Product Code EJI
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.6770
Decision Date 1984-07-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CITOJECT CARTRIDGE SYRINGE received FDA 510(k) clearance under submission number K842006, sponsored by Miles Laboratories, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1984-07-16.

Classification & Regulation

This clearance is catalogued under FDA product code EJI and 21 CFR 872.6770, within the Dental review panel as a Class II device.