meddevicedb.com FDA Device Reference

DISPOSABLE FILTERED INSUFFLATION TUBING SET

K941685 Class II Traditional
Decision Date
1994-05-26
Sponsor / Applicant
Blue Planet Industries, Inc.

Technical Specification

510(k) Submission ID K941685
Product Code HIF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1730
Decision Date 1994-05-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

DISPOSABLE FILTERED INSUFFLATION TUBING SET received FDA 510(k) clearance under submission number K941685, sponsored by Blue Planet Industries, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Obstetrics/Gynecology review panel. The statutory decision date of record is 1994-05-26.

Classification & Regulation

This clearance is catalogued under FDA product code HIF and 21 CFR 884.1730, within the Obstetrics/Gynecology review panel as a Class II device.