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MODEL 7-AT TREATMENT CHAMBER

K896721 Class II Traditional
Decision Date
1990-01-22
Sponsor / Applicant
J. H. Emerson Co.

Technical Specification

510(k) Submission ID K896721
Product Code LGM
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5450
Decision Date 1990-01-22
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MODEL 7-AT TREATMENT CHAMBER received FDA 510(k) clearance under submission number K896721, 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 1990-01-22.

Classification & Regulation

This clearance is catalogued under FDA product code LGM and 21 CFR 880.5450, within the General Hospital review panel as a Class II device.