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HORIZON 2000 ST ANALYSIS OPTION

K903524 Class II Traditional
Decision Date
1991-03-01
Sponsor / Applicant
Mennen Medical, Inc.

Technical Specification

510(k) Submission ID K903524
Product Code DPS
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2340
Decision Date 1991-03-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HORIZON 2000 ST ANALYSIS OPTION received FDA 510(k) clearance under submission number K903524, sponsored by Mennen Medical, 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 1991-03-01.

Classification & Regulation

This clearance is catalogued under FDA product code DPS and 21 CFR 870.2340, within the Cardiovascular review panel as a Class II device.