meddevicedb.com FDA Device Reference

CRYSTAL VISION AND ACCESSORIES

K932230 Class II Traditional
Decision Date
1994-02-18
Sponsor / Applicant
I.C Medical, Inc.

Technical Specification

510(k) Submission ID K932230
Product Code FYD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.5070
Decision Date 1994-02-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CRYSTAL VISION AND ACCESSORIES received FDA 510(k) clearance under submission number K932230, sponsored by I.C Medical, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1994-02-18.

Classification & Regulation

This clearance is catalogued under FDA product code FYD and 21 CFR 878.5070, within the General, Plastic Surgery review panel as a Class II device.