meddevicedb.com FDA Device Reference

HERAEUS LASERSONIC INC. STERILE DISPOSABLE FIBERS

K892211 Class II Traditional
Decision Date
1989-05-19
Sponsor / Applicant
Heraeus Lasersonics, Inc.

Technical Specification

510(k) Submission ID K892211
Product Code GEX
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4810
Decision Date 1989-05-19
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

HERAEUS LASERSONIC INC. STERILE DISPOSABLE FIBERS received FDA 510(k) clearance under submission number K892211, sponsored by Heraeus Lasersonics, 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 1989-05-19.

Classification & Regulation

This clearance is catalogued under FDA product code GEX and 21 CFR 878.4810, within the General, Plastic Surgery review panel as a Class II device.