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PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER

K883436 Class II Traditional
Decision Date
1988-10-17
Sponsor / Applicant
Ppg Industries, Inc.

Technical Specification

510(k) Submission ID K883436
Product Code DXO
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.2870
Decision Date 1988-10-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

PPG BIOMEDICAL FLEXIBLE MICRO TRANSDUCER CATHETER received FDA 510(k) clearance under submission number K883436, sponsored by Ppg Industries, 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 1988-10-17.

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.