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STONE EXTRACTOR

K971123 Class II Traditional
Decision Date
1997-06-27
Sponsor / Applicant
Phx Technologies Corp.

Technical Specification

510(k) Submission ID K971123
Product Code OCZ
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1500
Decision Date 1997-06-27
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

STONE EXTRACTOR received FDA 510(k) clearance under submission number K971123, sponsored by Phx Technologies Corp.. 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 1997-06-27.

Classification & Regulation

This clearance is catalogued under FDA product code OCZ and 21 CFR 876.1500, within the Gastroenterology, Urology review panel as a Class II device.