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ALARM, THERMAL, THERM-ALERT

K760683 Class II Traditional
Decision Date
1976-09-27
Sponsor / Applicant
Respiratory Care, Inc.

Technical Specification

510(k) Submission ID K760683
Product Code KPD
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2200
Decision Date 1976-09-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ALARM, THERMAL, THERM-ALERT received FDA 510(k) clearance under submission number K760683, sponsored by Respiratory Care, Inc.. 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 1976-09-27.

Classification & Regulation

This clearance is catalogued under FDA product code KPD and 21 CFR 880.2200, within the General Hospital review panel as a Class II device.