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LUNDERQUIST - RING PTC DRAINAGE CATHETER

K861220 Class II Traditional
Decision Date
1986-05-19
Sponsor / Applicant
Meadox Surgimed, Inc.

Technical Specification

510(k) Submission ID K861220
Product Code FGE
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5010
Decision Date 1986-05-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

LUNDERQUIST - RING PTC DRAINAGE CATHETER received FDA 510(k) clearance under submission number K861220, sponsored by Meadox Surgimed, Inc.. 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 1986-05-19.

Classification & Regulation

This clearance is catalogued under FDA product code FGE and 21 CFR 876.5010, within the Gastroenterology, Urology review panel as a Class II device.