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HEART RATE & TEMP. MEASUREMENT SYSTEM

K822939 Class II Traditional
Decision Date
1982-11-24
Sponsor / Applicant
Camino Laboratories, Inc.

Technical Specification

510(k) Submission ID K822939
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 1982-11-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HEART RATE & TEMP. MEASUREMENT SYSTEM received FDA 510(k) clearance under submission number K822939, sponsored by Camino Laboratories, 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 1982-11-24.

Classification & Regulation

This clearance is catalogued under FDA product code FLL and 21 CFR 880.2910, within the General Hospital review panel as a Class II device.