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DISPOSABLE CATHETER PRESSURE TRANSDUCER

K894033 Class II Traditional
Decision Date
1989-10-17
Sponsor / Applicant
Deseret Medical, Inc.

Technical Specification

510(k) Submission ID K894033
Product Code DXO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2870
Decision Date 1989-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE CATHETER PRESSURE TRANSDUCER received FDA 510(k) clearance under submission number K894033, sponsored by Deseret 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 1989-10-17.

Classification & Regulation

This clearance is catalogued under FDA product code DXO and 21 CFR 870.2870, within the Cardiovascular review panel as a Class II device.