meddevicedb.com FDA Device Reference

INSERTION

K920515 Class II Traditional
Decision Date
1992-05-04
Sponsor / Applicant
Accurate Surgical Instruments Co.

Technical Specification

510(k) Submission ID K920515
Product Code FJS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1992-05-04
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

INSERTION received FDA 510(k) clearance under submission number K920515, sponsored by Accurate Surgical Instruments 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 1992-05-04.

Classification & Regulation

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