meddevicedb.com FDA Device Reference

HTS *1

K822843 Class II Traditional
Decision Date
1982-12-15
Sponsor / Applicant
Global Office Automation System, Inc.

Technical Specification

510(k) Submission ID K822843
Product Code DSK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1110
Decision Date 1982-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HTS *1 received FDA 510(k) clearance under submission number K822843, sponsored by Global Office Automation System, 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 1982-12-15.

Classification & Regulation

This clearance is catalogued under FDA product code DSK and 21 CFR 870.1110, within the Cardiovascular review panel as a Class II device.