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TRIP TONOMETRY CATHETER, 8F

K992181 Class II Traditional
Decision Date
1999-08-24
Sponsor / Applicant
Datex-Ohmeda, Inc.

Technical Specification

510(k) Submission ID K992181
Product Code KNT
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5980
Decision Date 1999-08-24
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

TRIP TONOMETRY CATHETER, 8F received FDA 510(k) clearance under submission number K992181, sponsored by Datex-Ohmeda, 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 1999-08-24.

Classification & Regulation

This clearance is catalogued under FDA product code KNT and 21 CFR 876.5980, within the Gastroenterology, Urology review panel as a Class II device.