meddevicedb.com FDA Device Reference

ST-610 NEEDLESCOPE STERILIZATION TRAY

K823297 Class II Traditional
Decision Date
1983-05-06
Sponsor / Applicant
Medigroup

Technical Specification

510(k) Submission ID K823297
Product Code HET
Medical Specialty / Panel Obstetrics/Gynecology
Regulation Citation 21 CFR 884.1720
Decision Date 1983-05-06
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ST-610 NEEDLESCOPE STERILIZATION TRAY received FDA 510(k) clearance under submission number K823297, sponsored by Medigroup. 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 1983-05-06.

Classification & Regulation

This clearance is catalogued under FDA product code HET and 21 CFR 884.1720, within the Obstetrics/Gynecology review panel as a Class II device.