meddevicedb.com FDA Device Reference

R&D BATTERIES, PART NOS. 5135, 5097, 5444, AND 5502

K942034 Class II Traditional
Decision Date
1994-06-03
Sponsor / Applicant
R & D Batteries, Inc.

Technical Specification

510(k) Submission ID K942034
Product Code HLJ
Medical Specialty / Panel Ophthalmic
Regulation Citation 21 CFR 886.1570
Decision Date 1994-06-03
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

R&D BATTERIES, PART NOS. 5135, 5097, 5444, AND 5502 received FDA 510(k) clearance under submission number K942034, sponsored by R & D Batteries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Ophthalmic review panel. The statutory decision date of record is 1994-06-03.

Classification & Regulation

This clearance is catalogued under FDA product code HLJ and 21 CFR 886.1570, within the Ophthalmic review panel as a Class II device.