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MODEL 5650 OPTIMATE PERSONAL PROGRAMMER

K884522 Class III Traditional
Decision Date
1989-08-25
Sponsor / Applicant
Teletronics, Inc.

Technical Specification

510(k) Submission ID K884522
Product Code KRG
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.3700
Decision Date 1989-08-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 5650 OPTIMATE PERSONAL PROGRAMMER received FDA 510(k) clearance under submission number K884522, sponsored by Teletronics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1989-08-25.

Classification & Regulation

This clearance is catalogued under FDA product code KRG and 21 CFR 870.3700, within the Cardiovascular review panel as a Class III device.