meddevicedb.com FDA Device Reference

FIRST RESPONSE EMERG. MEDICSL - BURNS

K841898 Class I Traditional
Decision Date
1984-08-14
Sponsor / Applicant
Reed Products, Inc.

Technical Specification

510(k) Submission ID K841898
Product Code FPY
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5180
Decision Date 1984-08-14
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

FIRST RESPONSE EMERG. MEDICSL - BURNS received FDA 510(k) clearance under submission number K841898, sponsored by Reed Products, 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 1984-08-14.

Classification & Regulation

This clearance is catalogued under FDA product code FPY and 21 CFR 880.5180, within the General Hospital review panel as a Class I device.