meddevicedb.com FDA Device Reference

KENDALL-LTP DISPOSABLE TEMPERATURE PROBES (DTP1,DTP2,DTP3,DTP4)

K964401 Class II Traditional
Decision Date
1997-02-06
Sponsor / Applicant
Ludlow Technical Products

Technical Specification

510(k) Submission ID K964401
Product Code FMT
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5130
Decision Date 1997-02-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

KENDALL-LTP DISPOSABLE TEMPERATURE PROBES (DTP1,DTP2,DTP3,DTP4) received FDA 510(k) clearance under submission number K964401, sponsored by Ludlow Technical Products. 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 1997-02-06.

Classification & Regulation

This clearance is catalogued under FDA product code FMT and 21 CFR 880.5130, within the General Hospital review panel as a Class II device.