meddevicedb.com FDA Device Reference

TRANSDUCER FILTER

K821268 Class II Traditional
Decision Date
1982-06-23
Sponsor / Applicant
Cp Medical

Technical Specification

510(k) Submission ID K821268
Product Code FIB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 1982-06-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRANSDUCER FILTER received FDA 510(k) clearance under submission number K821268, sponsored by Cp Medical. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 1982-06-23.

Classification & Regulation

This clearance is catalogued under FDA product code FIB and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.