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QMS MAPPING SYSTEM,MODEL 2000

K990058 Class II Traditional
Decision Date
1999-12-15
Sponsor / Applicant
Cathdata, Inc.

Technical Specification

510(k) Submission ID K990058
Product Code DQK
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1425
Decision Date 1999-12-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

QMS MAPPING SYSTEM,MODEL 2000 received FDA 510(k) clearance under submission number K990058, sponsored by Cathdata, 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 1999-12-15.

Classification & Regulation

This clearance is catalogued under FDA product code DQK and 21 CFR 870.1425, within the Cardiovascular review panel as a Class II device.