meddevicedb.com FDA Device Reference

CATHETER BUBBLE STAND

K813487 Class II Traditional
Decision Date
1981-12-31
Sponsor / Applicant
Accurate Surgical Instruments Co.

Technical Specification

510(k) Submission ID K813487
Product Code FKX
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5630
Decision Date 1981-12-31
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CATHETER BUBBLE STAND received FDA 510(k) clearance under submission number K813487, 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 1981-12-31.

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.