meddevicedb.com FDA Device Reference

EMERSON THORACIC SUCTION REG. #55-JP

K820077 Class II Traditional
Decision Date
1982-01-28
Sponsor / Applicant
J. H. Emerson Co.

Technical Specification

510(k) Submission ID K820077
Product Code KDP
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.6740
Decision Date 1982-01-28
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EMERSON THORACIC SUCTION REG. #55-JP received FDA 510(k) clearance under submission number K820077, sponsored by J. H. Emerson Co.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 1982-01-28.

Classification & Regulation

This clearance is catalogued under FDA product code KDP and 21 CFR 880.6740, within the General Hospital review panel as a Class II device.