meddevicedb.com FDA Device Reference

ACC-U-THERM TEMPERATURE MONITOR

K813468 Class II Traditional
Decision Date
1982-01-07
Sponsor / Applicant
Diatek, Inc.

Technical Specification

510(k) Submission ID K813468
Product Code FLL
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.2910
Decision Date 1982-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ACC-U-THERM TEMPERATURE MONITOR received FDA 510(k) clearance under submission number K813468, sponsored by Diatek, 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 1982-01-07.

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.