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OTT INSUFFLATION FILTER TUBING

K920205 Class II Traditional
Decision Date
1993-10-25
Sponsor / Applicant
Georgia Biomedical Research Group, Inc.

Technical Specification

510(k) Submission ID K920205
Product Code HIF
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1730
Decision Date 1993-10-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OTT INSUFFLATION FILTER TUBING received FDA 510(k) clearance under submission number K920205, sponsored by Georgia Biomedical Research Group, 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 1993-10-25.

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.