meddevicedb.com FDA Device Reference

STERILE, DISPOS. SPIKE PROTECTOR-5C4138

K823777 Class II Traditional
Decision Date
1983-01-07
Sponsor / Applicant
Travenol Laboratories, S.A.

Technical Specification

510(k) Submission ID K823777
Product Code FKX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1983-01-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STERILE, DISPOS. SPIKE PROTECTOR-5C4138 received FDA 510(k) clearance under submission number K823777, sponsored by Travenol Laboratories, S.A.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1983-01-07.

Classification & Regulation

This clearance is catalogued under FDA product code FKX and 21 CFR 876.5630, within the Gastroenterology, Urology review panel as a Class II device.