meddevicedb.com FDA Device Reference

MEDSURG CIRCUMCISION TRAY

K920838 Class II Traditional
Decision Date
1993-10-15
Sponsor / Applicant
Medsurg Industries, Inc.

Technical Specification

510(k) Submission ID K920838
Product Code HFK
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.3900
Decision Date 1993-10-15
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

MEDSURG CIRCUMCISION TRAY received FDA 510(k) clearance under submission number K920838, sponsored by Medsurg 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 1993-10-15.

Classification & Regulation

This clearance is catalogued under FDA product code HFK and 21 CFR 884.3900, within the Obstetrics/Gynecology review panel as a Class II device.