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PHOENIX DISPOSABLE PRESSURE TRANSDUCER #73-600

K925638 Class II Traditional
Decision Date
1993-10-18
Sponsor / Applicant
Baxter Healthcare Corp

Technical Specification

510(k) Submission ID K925638
Product Code DXO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2870
Decision Date 1993-10-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PHOENIX DISPOSABLE PRESSURE TRANSDUCER #73-600 received FDA 510(k) clearance under submission number K925638, sponsored by Baxter Healthcare Corp. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 1993-10-18.

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.