meddevicedb.com FDA Device Reference

Celerity ECG Cable Accessory Pack

K171931 Class II Traditional
Decision Date
2017-10-26
Sponsor / Applicant
Medcomp (Medical Components, Inc.)

Technical Specification

510(k) Submission ID K171931
Product Code LJS
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5970
Decision Date 2017-10-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Celerity ECG Cable Accessory Pack received FDA 510(k) clearance under submission number K171931, sponsored by Medcomp (Medical Components, 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 2017-10-26.

Classification & Regulation

This clearance is catalogued under FDA product code LJS and 21 CFR 880.5970, within the General Hospital review panel as a Class II device.