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TRANSONIC FLOW-QC SET MODEL ADT1010

K021571 Class II Traditional
Decision Date
2002-08-12
Sponsor / Applicant
Transonic Systems, Inc.

Technical Specification

510(k) Submission ID K021571
Product Code MQS
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 2002-08-12
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRANSONIC FLOW-QC SET MODEL ADT1010 received FDA 510(k) clearance under submission number K021571, sponsored by Transonic Systems, Inc.. 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 2002-08-12.

Classification & Regulation

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