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GOLDEN-RULE SCALING CATHETER

K002416 Class II Traditional
Decision Date
2000-09-11
Sponsor / Applicant
Medical Device Technologies, Inc.

Technical Specification

510(k) Submission ID K002416
Product Code DQO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1200
Decision Date 2000-09-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GOLDEN-RULE SCALING CATHETER received FDA 510(k) clearance under submission number K002416, sponsored by Medical Device Technologies, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2000-09-11.

Classification & Regulation

This clearance is catalogued under FDA product code DQO and 21 CFR 870.1200, within the Cardiovascular review panel as a Class II device.