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CENTRAL STATION CONTROLLER AC100/CE100

K810169 Class I Traditional
Decision Date
1981-02-25
Sponsor / Applicant
Honeywell, Inc.

Technical Specification

510(k) Submission ID K810169
Product Code DSF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2810
Decision Date 1981-02-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CENTRAL STATION CONTROLLER AC100/CE100 received FDA 510(k) clearance under submission number K810169, sponsored by Honeywell, 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 1981-02-25.

Classification & Regulation

This clearance is catalogued under FDA product code DSF and 21 CFR 870.2810, within the Cardiovascular review panel as a Class I device.