meddevicedb.com FDA Device Reference

MANOMETRIC ASSEMBLIES

K983665 Class II Traditional
Decision Date
1999-05-17
Sponsor / Applicant
Dentsleeve Pty., Ltd.

Technical Specification

510(k) Submission ID K983665
Product Code KLA
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.1725
Decision Date 1999-05-17
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MANOMETRIC ASSEMBLIES received FDA 510(k) clearance under submission number K983665, sponsored by Dentsleeve Pty., Ltd.. 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 1999-05-17.

Classification & Regulation

This clearance is catalogued under FDA product code KLA and 21 CFR 876.1725, within the Gastroenterology, Urology review panel as a Class II device.