meddevicedb.com FDA Device Reference

EFFNER SIMS RECTAL SPECULUM W/FIBER OPTIC ILLUMINA

K852014 Class I Traditional
Decision Date
1985-08-07
Sponsor / Applicant
Effner and Spreine Co.

Technical Specification

510(k) Submission ID K852014
Product Code KOA
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4730
Decision Date 1985-08-07
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

EFFNER SIMS RECTAL SPECULUM W/FIBER OPTIC ILLUMINA received FDA 510(k) clearance under submission number K852014, sponsored by Effner and Spreine Co.. 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 1985-08-07.

Classification & Regulation

This clearance is catalogued under FDA product code KOA and 21 CFR 876.4730, within the Gastroenterology, Urology review panel as a Class I device.